A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050943



Internal ID19140162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:68414663..68511675hg38UCSC Ensembl
Innerchr10:70174420..70271432hg19UCSC Ensembl
Innerchr10:69844426..69941438hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3897013
hg1997013
hg1897013
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3517487
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)nsv1050943
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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