A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13753902



Internal ID5652325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35708569..35714249hg38UCSC Ensembl
Innerchr10:35708569..35714249hg38UCSC Ensembl
Outerchr10:35708452..35714396hg38UCSC Ensembl
chr10:35997497..36003177hg19UCSC Ensembl
Innerchr10:35997497..36003177hg19UCSC Ensembl
Outerchr10:35997380..36003324hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg385681
hg195681
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622905
Supporting Variants
SamplesNA19067
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13753902
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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