A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040432



Internal ID19129651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:31293973..31411280hg38UCSC Ensembl
Innerchr11:31315520..31432827hg19UCSC Ensembl
Innerchr11:31272096..31389403hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38117308
hg19117308
hg18117308
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3507668
Samples
Known GenesDCDC1, DNAJC24
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040432
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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