A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699155



Internal ID15435807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:19733142..19743467hg38UCSC Ensembl
Innerchr11:19754688..19765013hg19UCSC Ensembl
Innerchr11:19711264..19721589hg18UCSC Ensembl
Innerchr11:19711264..19721589hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3810326
hg1910326
hg1810326
hg1710326
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523404
Supporting Variants
Samples
Known GenesNAV2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699155
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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