A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3520573



Internal ID18472168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43074511..43095726hg38UCSC Ensembl
Innerchr10:43569959..43591174hg19UCSC Ensembl
Innerchr10:42889965..42911180hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3821216
hg1921216
hg1821216
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051646
Supporting Variants
Samples
Known GenesRET
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3520573
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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