A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695790



Internal ID15432442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:9637100..9648186hg38UCSC Ensembl
Innerchr2:9777229..9788315hg19UCSC Ensembl
Innerchr2:9694680..9705766hg18UCSC Ensembl
Innerchr2:9727827..9738913hg17UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3811087
hg1911087
hg1811087
hg1711087
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518363
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695790
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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