A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1107312



Internal ID15960498
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 StatusS
Merged Variantsnsv610681
Supporting Variants
Samples
Known GenesMTUS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1107312
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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