A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891809



Internal ID18839519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:50242444..50647850hg38UCSC Ensembl
Outerchr10:50242444..50647850hg38UCSC Ensembl
Innerchr10:52002204..52407610hg19UCSC Ensembl
Outerchr10:52002204..52407610hg19UCSC Ensembl
Innerchr10:51672210..52077616hg18UCSC Ensembl
Outerchr10:51672210..52077616hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38405407
hg19405407
hg18405407
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788425
Samples
Known GenesASAH2, SGMS1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891809
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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