A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686091



Internal ID15422743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:120375789..120554730hg38UCSC Ensembl
Innerchr7:120015843..120194784hg19UCSC Ensembl
Innerchr7:119803079..119982020hg18UCSC Ensembl
Innerchr7:119609794..119788735hg17UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38178942
hg19178942
hg18178942
hg17178942
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516686
Supporting Variants
Samples
Known GenesKCND2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv686091
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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