A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607615



Internal ID16048338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76516684..76819500hg38UCSC Ensembl
Innerchr7:76146001..76448817hg19UCSC Ensembl
Innerchr7:75983937..76286753hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38302817
hg19302817
hg18302817
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11465n54
Supporting Variantsnssv1088461
Samples
Known GenesLOC100133091, POMZP3, UPK3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607615
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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