A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606367



Internal ID16393776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:20423751..20528539hg38UCSC Ensembl
Innerchr7:20463374..20568162hg19UCSC Ensembl
Innerchr7:20429899..20534687hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38104789
hg19104789
hg18104789
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1079655
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606367
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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