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dbVar

Database of genomic structural variation

nsv5637326

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Ebert et al. 2021

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 106 SVs from 23 studies. See in: genome view

Submitted genomic77,042,346-77,042,346

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5637326	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	77,042,346	77,042,346
nsv5637326	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	76,338,171	76,338,171

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17156849	insertion	HG03371	Sequencing	Sequence alignment	2,852

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17156849	Submitted genomic		NC_000005.10:g.770 42346_77042347ins1 29	GRCh38 (hg38)		NC_000005.10	Chr5	77,042,346	77,042,346
nssv17156849	Remapped	Perfect	NC_000005.9:g.7633 8171_76338172ins12 9	GRCh37.p13	First Pass	NC_000005.9	Chr5	76,338,171	76,338,171

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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