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nsv5541660

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:30

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 202 SVs from 39 studies. See in: genome view    
Submitted genomic167,130,947-167,130,976Question Mark
Overlapping variant regions from other studies: 202 SVs from 39 studies. See in: genome view    
Remapped(Score: Perfect):167,544,435-167,544,464Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5541660Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6167,130,947167,130,976
nsv5541660RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6167,544,435167,544,464

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16991255insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16991255Submitted genomicNC_000006.12:g.167
130947_167130976in
s82
GRCh38 (hg38)NC_000006.12Chr6167,130,947167,130,976
nssv16991255RemappedPerfectNC_000006.11:g.167
544435_167544464in
s82
GRCh37.p13First PassNC_000006.11Chr6167,544,435167,544,464

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv169912550.0181106226
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