A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704965



Internal ID15094931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:34849610..34884725hg38UCSC Ensembl
Innerchr7:34889222..34924337hg19UCSC Ensembl
Innerchr7:34855747..34890862hg18UCSC Ensembl
Innerchr7:34662462..34697577hg17UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3835116
hg1935116
hg1835116
hg1735116
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528377
Supporting Variants
Samples
Known GenesNPSR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704965
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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