A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612174



Internal ID16399583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:128736472..128752184hg38UCSC Ensembl
Innerchr8:129748718..129764430hg19UCSC Ensembl
Innerchr8:129817900..129833612hg18UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3815713
hg1915713
hg1815713
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12310n54
Supporting Variantsnssv1120779
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612174
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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