A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606525



Internal ID16393934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:31256422..31279169hg38UCSC Ensembl
Innerchr7:31296036..31318783hg19UCSC Ensembl
Innerchr7:31262561..31285308hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3822748
hg1922748
hg1822748
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1081799
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606525
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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