A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065267



Internal ID18807798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46110126..46317042hg38UCSC Ensembl
Innerchr17:44187492..44394408hg19UCSC Ensembl
Innerchr17:41543275..41750183hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38206917
hg19206917
hg18206909
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3184n100
Supporting Variantsnssv3548602
Samples
Known GenesARL17A, ARL17B, KANSL1, KANSL1-AS1, LOC644172, LRRC37A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065267
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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