A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037679



Internal ID19126898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:68493125..68695174hg38UCSC Ensembl
Innerchr10:70252882..70454931hg19UCSC Ensembl
Innerchr10:69922888..70124937hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38202050
hg19202050
hg18202050
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3505244
Samples
Known GenesSLC25A16, TET1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037679
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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