A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604445



Internal ID16391854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:107114286..107115255hg38UCSC Ensembl
Innerchr6:107435490..107436459hg19UCSC Ensembl
Innerchr6:107542183..107543152hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38970
hg19970
hg18970
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1071895
Samples
Known GenesBEND3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604445
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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