A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3415799



Internal ID14916072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26640952..26944612hg38UCSC Ensembl
Innerchr10:26641002..26944562hg38UCSC Ensembl
Outerchr10:26640902..26944662hg38UCSC Ensembl
chr10:26929881..27233541hg19UCSC Ensembl
Innerchr10:26929931..27233491hg19UCSC Ensembl
Outerchr10:26929831..27233591hg19UCSC Ensembl
chr10:26969887..27273547hg18UCSC Ensembl
Innerchr10:26969937..27273497hg18UCSC Ensembl
Outerchr10:26969837..27273597hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38303661
hg19303661
hg18303661
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8740695
SamplesNA19240
Known GenesABI1, LINC00202-1, LINC00202-2, PDSS1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3415799
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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