A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156377



Internal ID15873210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:114215638..114268612hg38UCSC Ensembl
Innerchr8:115227867..115280841hg19UCSC Ensembl
Innerchr8:115297043..115350017hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3852975
hg1952975
hg1852975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611973
Supporting Variants
SamplesHGDP00144
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156377
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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