A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611411



Internal ID16398820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:57923080..57966227hg38UCSC Ensembl
Innerchr8:58835639..58878786hg19UCSC Ensembl
Innerchr8:58998193..59041340hg18UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3843148
hg1943148
hg1843148
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1115604
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611411
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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