A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058898



Internal ID18801429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46099606..46582828hg38UCSC Ensembl
Innerchr17:44176972..44660194hg19UCSC Ensembl
Innerchr17:41532785..42015510hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38483223
hg19483223
hg18482726
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3188n100
Supporting Variantsnssv3548521
Samples
Known GenesARL17A, ARL17B, KANSL1, KANSL1-AS1, LOC644172, LRRC37A, LRRC37A2, NSFP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058898
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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