A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609112



Internal ID16396521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:154738892..154760633hg38UCSC Ensembl
Innerchr7:154530602..154552343hg19UCSC Ensembl
Innerchr7:154161535..154183276hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3821742
hg1921742
hg1821742
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1100253
Samples
Known GenesDPP6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609112
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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