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dbVar

Database of genomic structural variation

nsv4753359

Organism: Homo sapiens

Study:nstd199 (Quan et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh37

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

Publication(s):Quan 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: 104 SVs from 27 studies. See in: genome view

Remapped(Score: Perfect):10,377,632-10,377,632

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4753359	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000019.10	Chr19	10,377,632	10,377,632
nsv4753359	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000019.9	Chr19	10,488,308	10,488,308

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16286613	insertion	Sequencing	Split read mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16286613	Remapped	Perfect	NC_000019.10:g.103 77632_10377633ins2 86	GRCh38.p12	First Pass	NC_000019.10	Chr19	10,377,632	10,377,632
nssv16286613	Submitted genomic		NC_000019.9:g.1048 8308_10488309ins28 6	GRCh37 (hg19)		NC_000019.9	Chr19	10,488,308	10,488,308

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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