A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611823



Internal ID16399232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:102941762..102967486hg38UCSC Ensembl
Innerchr8:103953990..103979714hg19UCSC Ensembl
Innerchr8:104023166..104048890hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3825725
hg1925725
hg1825725
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156144
Samples1780862484_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611823
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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