A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13728169



Internal ID6539205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25898912..25903165hg38UCSC Ensembl
Innerchr10:25898912..25903165hg38UCSC Ensembl
Outerchr10:25898668..25903424hg38UCSC Ensembl
chr10:26187841..26192094hg19UCSC Ensembl
Innerchr10:26187841..26192094hg19UCSC Ensembl
Outerchr10:26187597..26192353hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg384254
hg194254
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622681
Supporting Variants
SamplesNA20586
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13728169
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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