A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045343



Internal ID19134562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:68853524..68866574hg38UCSC Ensembl
Innerchr10:70613280..70626330hg19UCSC Ensembl
Innerchr10:70283286..70296336hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3813051
hg1913051
hg1813051
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3508150
Samples
Known GenesSTOX1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045343
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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