A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610452



Internal ID16051175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:13799452..14103624hg38UCSC Ensembl
Innerchr8:13656961..13961133hg19UCSC Ensembl
Innerchr8:13701332..14005504hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38304173
hg19304173
hg18304173
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1106806
Samples
Known GenesSGCZ
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610452
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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