A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606167



Internal ID16393576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:9640892..9836850hg38UCSC Ensembl
Innerchr7:9680522..9876479hg19UCSC Ensembl
Innerchr7:9647047..9843004hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38195959
hg19195958
hg18195958
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1079123
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606167
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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