A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695013



Internal ID15431665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:88473430..88519150hg38UCSC Ensembl
Innerchr7:88102745..88148465hg19UCSC Ensembl
Innerchr7:87940681..87986401hg18UCSC Ensembl
Innerchr7:87747396..87793116hg17UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg3845721
hg1945721
hg1845721
hg1745721
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522235
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695013
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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