A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609132



Internal ID16396541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155345740..155350604hg38UCSC Ensembl
Innerchr7:155138440..155143235hg19UCSC Ensembl
Innerchr7:154831196..154836060hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg384865
hg194796
hg184865
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11747n54
Supporting Variantsnssv1100276
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609132
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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