A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603578



Internal ID16390987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:66658257..66739071hg38UCSC Ensembl
Innerchr6:67368150..67448964hg19UCSC Ensembl
Innerchr6:67424871..67505685hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3880815
hg1980815
hg1880815
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154797
SamplesNINDS_73
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603578
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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