A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528979



Internal ID15456272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:126957304..126967034hg38UCSC Ensembl
Innerchr2:127714880..127724610hg19UCSC Ensembl
Innerchr2:127431350..127441080hg18UCSC Ensembl
Innerchr2:127431110..127440840hg17UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg389731
hg199731
hg189731
hg179731
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705678
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528979
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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