A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065087



Internal ID19154306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:73745262..73767743hg38UCSC Ensembl
Innerchr17:71741401..71763882hg19UCSC Ensembl
Innerchr17:69252996..69275477hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3822482
hg1922482
hg1822482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3281n100
Supporting Variantsnssv3567777
Samples
Known GenesLINC00469, LOC100134391
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065087
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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