A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13725657



Internal ID374838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25859964..25865440hg38UCSC Ensembl
Innerchr10:25859964..25865440hg38UCSC Ensembl
Outerchr10:25859464..25865940hg38UCSC Ensembl
chr10:26148893..26154369hg19UCSC Ensembl
Innerchr10:26148893..26154369hg19UCSC Ensembl
Outerchr10:26148393..26154869hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg385477
hg195477
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622676
Supporting Variants
SamplesHG00108
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13725657
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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