A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155717



Internal ID15877643
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 StatusS
Merged Variantsnsv609093
Supporting Variants
SamplesHGDP01021
Known GenesDPP6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155717
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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