A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526400



Internal ID15453693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:133893655..133901914hg38UCSC Ensembl
Innerchr2:134651226..134659485hg19UCSC Ensembl
Innerchr2:134367696..134375955hg18UCSC Ensembl
Innerchr2:134484958..134493217hg17UCSC Ensembl
Cytoband2q21.2
Allele length
AssemblyAllele length
hg388260
hg198260
hg188260
hg178260
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702699
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526400
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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