A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611885



Internal ID16399294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:110975569..111151572hg38UCSC Ensembl
Innerchr8:111987798..112163801hg19UCSC Ensembl
Innerchr8:112056974..112232977hg18UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg38176004
hg19176004
hg18176004
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12260n54
Supporting Variantsnssv1118321
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611885
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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