A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610205



Internal ID16050928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8941601..9034134hg38UCSC Ensembl
Innerchr8:8799111..8891644hg19UCSC Ensembl
Innerchr8:8836521..8929054hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3892534
hg1992534
hg1892534
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1105988
Samples
Known GenesERI1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610205
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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