A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610681



Internal ID16398090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:17721626..17724191hg38UCSC Ensembl
Innerchr8:17579135..17581700hg19UCSC Ensembl
Innerchr8:17623415..17625980hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg382566
hg192566
hg182566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1107312
Samples
Known GenesMTUS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610681
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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