A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3359704



Internal ID14859966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1396657..1398355hg38UCSC Ensembl
Innerchr10:1397355..1397657hg38UCSC Ensembl
Outerchr10:1395657..1399355hg38UCSC Ensembl
chr10:1438852..1440550hg19UCSC Ensembl
Innerchr10:1439550..1439852hg19UCSC Ensembl
Outerchr10:1437852..1441550hg19UCSC Ensembl
chr10:1428852..1430550hg18UCSC Ensembl
Innerchr10:1429852..1429550hg18UCSC Ensembl
Outerchr10:1427852..1431550hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg381699
hg191699
hg181699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv344e59
Supporting Variantsessv8687990
SamplesNA19239
Known GenesADARB2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3359704
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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