A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066943



Internal ID18809474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46137522..46596297hg38UCSC Ensembl
Innerchr17:44214888..44673663hg19UCSC Ensembl
Innerchr17:41570665..42028979hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38458776
hg19458776
hg18458315
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3188n100
Supporting Variantsnssv3556562, nssv3556561
Samples
Known GenesARL17A, ARL17B, KANSL1, KANSL1-AS1, LOC644172, LRRC37A, LRRC37A2, NSF, NSFP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066943
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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