A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624024



Internal ID7010880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:83874902..83883500hg38UCSC Ensembl
Innerchr10:83874902..83883500hg38UCSC Ensembl
Outerchr10:83874402..83884000hg38UCSC Ensembl
chr10:85634658..85643256hg19UCSC Ensembl
Innerchr10:85634658..85643256hg19UCSC Ensembl
Outerchr10:85634158..85643756hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg388599
hg198599
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13880317
SamplesHG00524
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624024
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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