A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1115736



Internal ID15622236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:67074655..67104247hg38UCSC Ensembl
Innerchr8:67986890..68016482hg19UCSC Ensembl
Innerchr8:68149444..68179036hg18UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg3829593
hg1929593
hg1829593
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611458
Supporting Variants
Samples
Known GenesCSPP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1115736
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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