A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695774



Internal ID15432426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:42113019..42117753hg38UCSC Ensembl
Innerchr11:42134569..42139303hg19UCSC Ensembl
Innerchr11:42091145..42095879hg18UCSC Ensembl
Innerchr11:42091145..42095879hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg384735
hg194735
hg184735
hg174735
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518346
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695774
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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