A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13690268



Internal ID3433871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8023935..8025356hg38UCSC Ensembl
Innerchr10:8023936..8025355hg38UCSC Ensembl
Outerchr10:8023934..8025357hg38UCSC Ensembl
chr10:8065898..8067319hg19UCSC Ensembl
Innerchr10:8065899..8067318hg19UCSC Ensembl
Outerchr10:8065897..8067320hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381422
hg191422
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622281
Supporting Variants
SamplesHG03066
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13690268
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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