A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700468



Internal ID15437120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62565594..62575192hg38UCSC Ensembl
Innerchr7:62025972..62035570hg19UCSC Ensembl
Innerchr7:61663407..61673005hg18UCSC Ensembl
Innerchr7:61470122..61479720hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg389599
hg199599
hg189599
hg179599
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516283
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700468
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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