A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1091901



Internal ID15945087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:101361258..101367182hg38UCSC Ensembl
Innerchr7:101004539..101010463hg19UCSC Ensembl
Innerchr7:100791259..100797183hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg385925
hg195925
hg185925
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607983
Supporting Variants
Samples
Known GenesCOL26A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1091901
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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