A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13690313



Internal ID2440491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8086608..8087809hg38UCSC Ensembl
Innerchr10:8086621..8087796hg38UCSC Ensembl
Outerchr10:8086595..8087822hg38UCSC Ensembl
chr10:8128571..8129772hg19UCSC Ensembl
Innerchr10:8128584..8129759hg19UCSC Ensembl
Outerchr10:8128558..8129785hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381202
hg191202
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622282
Supporting Variants
SamplesHG02150
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13690313
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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