A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699013



Internal ID15435665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:101325082..101336029hg38UCSC Ensembl
Innerchr7:100968363..100979310hg19UCSC Ensembl
Innerchr7:100755083..100766030hg18UCSC Ensembl
Innerchr7:100561798..100572745hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3810948
hg1910948
hg1810948
hg1710948
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517175
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699013
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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