A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603377



Internal ID16390786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:63952818..63958196hg38UCSC Ensembl
Innerchr6:64662711..64668089hg19UCSC Ensembl
Innerchr6:64720670..64726048hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg385379
hg195379
hg185379
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10717n54
Supporting Variantsnssv1061465
Samples
Known GenesEYS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603377
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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