A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1071892



Internal ID15925078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:107114286..107114969hg38UCSC Ensembl
Innerchr6:107435490..107436173hg19UCSC Ensembl
Innerchr6:107542183..107542866hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38684
hg19684
hg18684
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604442
Supporting Variants
Samples
Known GenesBEND3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1071892
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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