A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040326



Internal ID19129545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:22841980..22872625hg38UCSC Ensembl
Innerchr11:22863526..22894171hg19UCSC Ensembl
Innerchr11:22820102..22850747hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3830646
hg1930646
hg1830646
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710059, nssv3507192
Samples
Known GenesCCDC179
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040326
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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