A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051520



Internal ID18794051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:68428357..68695174hg38UCSC Ensembl
Innerchr10:70188114..70454931hg19UCSC Ensembl
Innerchr10:69858120..70124937hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38266818
hg19266818
hg18266818
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv919n100
Supporting Variantsnssv3520450
Samples
Known GenesDNA2, SLC25A16, TET1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051520
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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