A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603760



Internal ID16391169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:74833001..74873670hg38UCSC Ensembl
Innerchr6:75542717..75583386hg19UCSC Ensembl
Innerchr6:75599437..75640106hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3840670
hg1940670
hg1840670
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10784n54
Supporting Variantsnssv1064516
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603760
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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