A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603633



Internal ID16391042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:69038708..69084187hg38UCSC Ensembl
Innerchr6:69748600..69794079hg19UCSC Ensembl
Innerchr6:69805321..69850800hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3845480
hg1945480
hg1845480
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10757n54
Supporting Variantsnssv1063659
Samples
Known GenesBAI3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603633
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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