A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623501



Internal ID7010357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62824994..62826834hg38UCSC Ensembl
Innerchr10:62824994..62826834hg38UCSC Ensembl
Outerchr10:62824866..62826959hg38UCSC Ensembl
chr10:64584754..64586594hg19UCSC Ensembl
Innerchr10:64584754..64586594hg19UCSC Ensembl
Outerchr10:64584626..64586719hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381841
hg191841
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13835129
SamplesNA19917
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623501
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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