A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066023



Internal ID18808554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15703953..16150198hg38UCSC Ensembl
Innerchr17:15607267..16053512hg19UCSC Ensembl
Innerchr17:15547992..15994237hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38446246
hg19446246
hg18446246
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3107n100
Supporting Variantsnssv3560422
Samples
Known GenesADORA2B, CDRT15P2, MEIS3P1, NCOR1, TBC1D26, TTC19, ZNF286A, ZSWIM7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066023
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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