A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1109161



Internal ID15615661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:25212386..25213120hg38UCSC Ensembl
Innerchr8:25069902..25070636hg19UCSC Ensembl
Innerchr8:25125819..25126553hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38735
hg19735
hg18735
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610833
Supporting Variants
Samples
Known GenesDOCK5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1109161
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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