A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1092080



Internal ID15945266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:107320070..107423241hg38UCSC Ensembl
Innerchr7:106960515..107063686hg19UCSC Ensembl
Innerchr7:106747751..106850922hg18UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38103172
hg19103172
hg18103172
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608073
Supporting Variants
Samples
Known GenesCOG5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1092080
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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