A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523864



Internal ID15451157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:126728469..126731237hg38UCSC Ensembl
Innerchr11:126598364..126601132hg19UCSC Ensembl
Innerchr11:126103574..126106342hg18UCSC Ensembl
Innerchr11:126103574..126106342hg17UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg382769
hg192769
hg182769
hg172769
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699701
Samples
Known GenesKIRREL3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523864
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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