A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv771011



Internal ID16064967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:31372799..31375881hg38UCSC Ensembl
Innerchr11:31394346..31397428hg19UCSC Ensembl
Innerchr11:31350922..31354004hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg383083
hg193083
hg183083
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553968
Supporting Variants
Samples
Known GenesDNAJC24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv771011
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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