A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603579



Internal ID16390988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:66674675..67939609hg38UCSC Ensembl
Innerchr6:67384568..68649501hg19UCSC Ensembl
Innerchr6:67441289..68706222hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg381264935
hg191264934
hg181264934
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1063556, nssv1063557
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603579
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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