A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1071889



Internal ID15578389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:107059633..107087381hg38UCSC Ensembl
Innerchr6:107380837..107408585hg19UCSC Ensembl
Innerchr6:107487530..107515278hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3827749
hg1927749
hg1827749
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604440
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)nssv1071889
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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