A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697581



Internal ID15434233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:201249214..201264623hg38UCSC Ensembl
Innerchr1:201218342..201233751hg19UCSC Ensembl
Innerchr1:199484965..199500374hg18UCSC Ensembl
Innerchr1:197949999..197965408hg17UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3815410
hg1915410
hg1815410
hg1715410
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520734
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697581
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer