A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657010



Internal ID15393662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13780343..13802173hg38UCSC Ensembl
Innerchr7:13819968..13841798hg19UCSC Ensembl
Innerchr7:13786493..13808323hg18UCSC Ensembl
Innerchr7:13593208..13615038hg17UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3821831
hg1921831
hg1821831
hg1721831
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519601
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657010
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