A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606235



Internal ID16393644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:12741756..13166325hg38UCSC Ensembl
Innerchr7:12781381..13205950hg19UCSC Ensembl
Innerchr7:12747906..13172475hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38424570
hg19424570
hg18424570
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1079187
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606235
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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