A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607025



Internal ID16394434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:54197894..54344915hg38UCSC Ensembl
Innerchr7:54265587..54412608hg19UCSC Ensembl
Innerchr7:54233081..54380102hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38147022
hg19147022
hg18147022
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11352n54
Supporting Variantsnssv1154969
SamplesHGDP00066
Known GenesHPVC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607025
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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