A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695879



Internal ID15432531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:21077898..21082715hg38UCSC Ensembl
Innerchr2:21300770..21305587hg19UCSC Ensembl
Innerchr2:21154275..21159092hg18UCSC Ensembl
Innerchr2:21212422..21217239hg17UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg384818
hg194818
hg184818
hg174818
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518443
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695879
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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