A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13714413



Internal ID1464957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:20573444..20604654hg38UCSC Ensembl
Innerchr10:20573444..20604654hg38UCSC Ensembl
Outerchr10:20572944..20605154hg38UCSC Ensembl
chr10:20862373..20893583hg19UCSC Ensembl
Innerchr10:20862373..20893583hg19UCSC Ensembl
Outerchr10:20861873..20894083hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3831211
hg1931211
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622562
Supporting Variants
SamplesHG01353
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13714413
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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