A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1120436



Internal ID15973622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:119145344..119153018hg38UCSC Ensembl
Innerchr8:120157583..120165257hg19UCSC Ensembl
Innerchr8:120226764..120234438hg18UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg387675
hg197675
hg187675
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612107
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1120436
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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