A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609143



Internal ID16396552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155345856..155350553hg38UCSC Ensembl
Innerchr7:155138556..155143184hg19UCSC Ensembl
Innerchr7:154831312..154836009hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg384698
hg194629
hg184698
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11747n54
Supporting Variantsnssv1100317
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609143
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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