A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13829048



Internal ID662291
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623433
Supporting Variants
SamplesHG00308
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13829048
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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