A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653133



Internal ID15043099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:128513182..128517527hg38UCSC Ensembl
Innerchr11:128383077..128387422hg19UCSC Ensembl
Innerchr11:127888287..127892632hg18UCSC Ensembl
Innerchr11:127888287..127892632hg17UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg384346
hg194346
hg184346
hg174346
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517012
Supporting Variants
Samples
Known GenesETS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv653133
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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