A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065712



Internal ID18808243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46137522..46351303hg38UCSC Ensembl
Innerchr17:44214888..44428669hg19UCSC Ensembl
Innerchr17:41570665..41784425hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38213782
hg19213782
hg18213761
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3185n100
Supporting Variantsnssv3556533, nssv3556532
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)nsv1065712
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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