A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043169



Internal ID19132388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:68441868..68493125hg38UCSC Ensembl
Innerchr10:70201625..70252882hg19UCSC Ensembl
Innerchr10:69871631..69922888hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3851258
hg1951258
hg1851258
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv920n100
Supporting Variantsnssv3514861
Samples
Known GenesDNA2, SLC25A16
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043169
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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