A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058933



Internal ID18801464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36589879..36644869hg38UCSC Ensembl
Innerchr17:34946309..35001325hg19UCSC Ensembl
Innerchr17:32020422..32075438hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3854991
hg1955017
hg1855017
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3156n100
Supporting Variantsnssv3562537
Samples
Known GenesDHRS11, MRM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058933
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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