A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061289



Internal ID18803820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46124010..46323689hg38UCSC Ensembl
Innerchr17:44201376..44401055hg19UCSC Ensembl
Innerchr17:41557154..41756820hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38199680
hg19199680
hg18199667
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3209n100
Supporting Variantsnssv3549848
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)nsv1061289
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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