A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611831



Internal ID16399240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:102983396..102990436hg38UCSC Ensembl
Innerchr8:103995624..104002664hg19UCSC Ensembl
Innerchr8:104064800..104071840hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg387041
hg197041
hg187041
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1118225
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611831
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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