A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv770674



Internal ID15717944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:31296288..31518040hg38UCSC Ensembl
Innerchr11:31317835..31539587hg19UCSC Ensembl
Innerchr11:31274411..31496163hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38221753
hg19221753
hg18221753
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553949
Supporting Variants
Samples
Known GenesDCDC1, DNAJC24, ELP4, IMMP1L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv770674
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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