A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1105889



Internal ID15959075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8349823..8374627hg38UCSC Ensembl
Innerchr8:8207339..8232143hg19UCSC Ensembl
Innerchr8:8244749..8269553hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3824805
hg1924805
hg1824805
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610157
Supporting Variants
Samples
Known GenesSGK223
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1105889
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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