A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062575



Internal ID18805106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46137522..46358076hg38UCSC Ensembl
Innerchr17:44214888..44435442hg19UCSC Ensembl
Innerchr17:41570665..41791184hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38220555
hg19220555
hg18220520
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3214n100
Supporting Variantsnssv3724011, nssv3556534, nssv3724012
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)nsv1062575
Frequency
Sample Size29084
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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