A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666505



Internal ID15403157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:97759718..97793614hg38UCSC Ensembl
Innerchr7:97389030..97422926hg19UCSC Ensembl
Innerchr7:97226966..97260862hg18UCSC Ensembl
Innerchr7:97033681..97067577hg17UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3833897
hg1933897
hg1833897
hg1733897
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516307
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv666505
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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