A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702701



Internal ID15439353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:68433827..68449952hg38UCSC Ensembl
Innerchr11:68201295..68217420hg19UCSC Ensembl
Innerchr11:67957871..67973996hg18UCSC Ensembl
Innerchr11:67957871..67973996hg17UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3816126
hg1916126
hg1816126
hg1716126
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526402
Supporting Variants
Samples
Known GenesLRP5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702701
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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