A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3513771



Internal ID18812052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43492825..43527025hg38UCSC Ensembl
Innerchr10:43988273..44022473hg19UCSC Ensembl
Innerchr10:43308279..43342479hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3834201
hg1934201
hg1834201
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051325
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3513771
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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