A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696168



Internal ID15432820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76577893..76599932hg38UCSC Ensembl
Innerchr11:76288937..76310976hg19UCSC Ensembl
Innerchr11:75966585..75988624hg18UCSC Ensembl
Innerchr11:75966585..75988624hg17UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3822040
hg1922040
hg1822040
hg1722040
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518717
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696168
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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