A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1106772



Internal ID15613272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:13093516..14267300hg38UCSC Ensembl
Innerchr8:12951025..14124809hg19UCSC Ensembl
Innerchr8:12995396..14169180hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg381173785
hg191173785
hg181173785
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610411
Supporting Variants
Samples
Known GenesC8orf48, DLC1, SGCZ
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1106772
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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