A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059370



Internal ID18801901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46130778..46708304hg38UCSC Ensembl
Innerchr17:44208144..44785670hg19UCSC Ensembl
Innerchr17:41563921..42140851hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38577527
hg19577527
hg18576931
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3188n100
Supporting Variantsnssv3549952
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)nsv1059370
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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