A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1088038



Internal ID15594538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76514388..76927895hg38UCSC Ensembl
Innerchr7:76143705..76557212hg19UCSC Ensembl
Innerchr7:75981641..76395148hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38413508
hg19413508
hg18413508
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607597
Supporting Variants
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)nssv1088038
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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