A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703562



Internal ID15093528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:93676638..93677987hg38UCSC Ensembl
Innerchr11:93409804..93411153hg19UCSC Ensembl
Innerchr11:93049452..93050801hg18UCSC Ensembl
Innerchr11:93049452..93050801hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg381350
hg191350
hg181350
hg171350
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527168
Supporting Variants
Samples
Known GenesKIAA1731
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703562
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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