A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13835129



Internal ID6317960
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623501
Supporting Variants
SamplesNA19917
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13835129
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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