A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv655057



Internal ID15045023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:45901139..45961834hg38UCSC Ensembl
Innerchr11:45922690..45983385hg19UCSC Ensembl
Innerchr11:45879266..45939961hg18UCSC Ensembl
Innerchr11:45879266..45939961hg17UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3860696
hg1960696
hg1860696
hg1760696
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516442
Supporting Variants
Samples
Known GenesC11orf94, GYLTL1B, MAPK8IP1, PEX16, PHF21A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv655057
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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