A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606424



Internal ID16047147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:24942910..25426902hg38UCSC Ensembl
Innerchr7:24982529..25466521hg19UCSC Ensembl
Innerchr7:24949054..25433046hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38483993
hg19483993
hg18483993
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1081139
Samples
Known GenesC7orf31, CYCS, NPVF, OSBPL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606424
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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