A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523257



Internal ID15450550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:159611597..159612428hg38UCSC Ensembl
Innerchr1:159581387..159582218hg19UCSC Ensembl
Innerchr1:157848011..157848842hg18UCSC Ensembl
Innerchr1:156394460..156395291hg17UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg38832
hg19832
hg18832
hg17832
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698987
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523257
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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