A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665706



Internal ID15402358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:136822664..136989767hg38UCSC Ensembl
Innerchr2:137580234..137747337hg19UCSC Ensembl
Innerchr2:137296704..137463807hg18UCSC Ensembl
Innerchr2:137413966..137581069hg17UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg38167104
hg19167104
hg18167104
hg17167104
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516011
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665706
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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