A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699831



Internal ID15436483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:126184390..126187449hg38UCSC Ensembl
Innerchr11:126054285..126057344hg19UCSC Ensembl
Innerchr11:125559495..125562554hg18UCSC Ensembl
Innerchr11:125559495..125562554hg17UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg383060
hg193060
hg183060
hg173060
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523976
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699831
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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