A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609093



Internal ID16396502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:154276796..154382550hg38UCSC Ensembl
Innerchr7:153973881..154079635hg19UCSC Ensembl
Innerchr7:153604814..153710568hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg38105755
hg19105755
hg18105755
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155717
SamplesHGDP01021
Known GenesDPP6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609093
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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