A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524626



Internal ID15451919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:43982585..43999763hg38UCSC Ensembl
Innerchr11:44004135..44021313hg19UCSC Ensembl
Innerchr11:43960711..43977889hg18UCSC Ensembl
Innerchr11:43960711..43977889hg17UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3817179
hg1917179
hg1817179
hg1717179
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700588
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524626
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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