A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037488



Internal ID18780019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43066585..43094479hg38UCSC Ensembl
Innerchr10:43562033..43589927hg19UCSC Ensembl
Innerchr10:42882039..42909933hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3827895
hg1927895
hg1827895
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv724n100
Supporting Variantsnssv3505042
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)nsv1037488
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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