A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058185



Internal ID18800716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:40473087..40533656hg38UCSC Ensembl
Innerchr17:38629339..38689908hg19UCSC Ensembl
Innerchr17:35882865..35943434hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3860570
hg1960570
hg1860570
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3562552
Samples
Known GenesTNS4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058185
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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