A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656695



Internal ID15046661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:44258540..44271197hg38UCSC Ensembl
Innerchr11:44280090..44292747hg19UCSC Ensembl
Innerchr11:44236666..44249323hg18UCSC Ensembl
Innerchr11:44236666..44249323hg17UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3812658
hg1912658
hg1812658
hg1712658
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517357
Supporting Variants
Samples
Known GenesALX4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656695
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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