A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623433



Internal ID7010290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:58330189..58334905hg38UCSC Ensembl
Innerchr10:58330206..58334889hg38UCSC Ensembl
Outerchr10:58330173..58334922hg38UCSC Ensembl
chr10:60089949..60094665hg19UCSC Ensembl
Innerchr10:60089966..60094649hg19UCSC Ensembl
Outerchr10:60089933..60094682hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg384717
hg194717
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13829049, essv13829051, essv13829050, essv13829048
SamplesHG00323, NA21119, HG03914, HG00308
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623433
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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