A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608339



Internal ID16395748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:124290495..124354577hg38UCSC Ensembl
Innerchr7:123930549..123994631hg19UCSC Ensembl
Innerchr7:123717785..123781867hg18UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3864083
hg1964083
hg1864083
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1093600
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608339
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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