A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606713



Internal ID16394122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:40332994..40388803hg38UCSC Ensembl
Innerchr7:40372593..40428402hg19UCSC Ensembl
Innerchr7:40339118..40394927hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3855810
hg1955810
hg1855810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11291n54
Supporting Variantsnssv1083049
Samples
Known GenesC7orf10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606713
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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