A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv684390



Internal ID15074356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:128513182..128518878hg38UCSC Ensembl
Innerchr11:128383077..128388773hg19UCSC Ensembl
Innerchr11:127888287..127893983hg18UCSC Ensembl
Innerchr11:127888287..127893983hg17UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg385697
hg195697
hg185697
hg175697
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)nssv684390
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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