A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525639



Internal ID15106246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:93672897..93677987hg38UCSC Ensembl
Innerchr11:93406063..93411153hg19UCSC Ensembl
Innerchr11:93045711..93050801hg18UCSC Ensembl
Innerchr11:93045711..93050801hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg385091
hg195091
hg185091
hg175091
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701793
Samples
Known GenesKIAA1731
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525639
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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