A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609104



Internal ID16396513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:154639470..154658116hg38UCSC Ensembl
Innerchr7:154431180..154449826hg19UCSC Ensembl
Innerchr7:154062113..154080759hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3818647
hg1918647
hg1818647
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1100233
Samples
Known GenesDPP6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609104
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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