A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608333



Internal ID16395742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:121492159..121739562hg38UCSC Ensembl
Innerchr7:121132213..121379616hg19UCSC Ensembl
Innerchr7:120919449..121166852hg18UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg38247404
hg19247404
hg18247404
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1093594
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608333
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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