A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661188



Internal ID15397840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:76318067..76361816hg38UCSC Ensembl
Innerchr2:76545193..76588942hg19UCSC Ensembl
Innerchr2:76398701..76442450hg18UCSC Ensembl
Innerchr2:76456848..76500597hg17UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3843750
hg1943750
hg1843750
hg1743750
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519947
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661188
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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