A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526169



Internal ID15453462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:120514073..120523027hg38UCSC Ensembl
Innerchr2:121271649..121280603hg19UCSC Ensembl
Innerchr2:120988119..120997073hg18UCSC Ensembl
Innerchr2:120987879..120996833hg17UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg388955
hg198955
hg188955
hg178955
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702430
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526169
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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