A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611873



Internal ID16399282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:107718165..107770770hg38UCSC Ensembl
Innerchr8:108730393..108782998hg19UCSC Ensembl
Innerchr8:108799569..108852174hg18UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3852606
hg1952606
hg1852606
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1118307
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611873
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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