A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13694188



Internal ID3404026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9701276..9735465hg38UCSC Ensembl
Innerchr10:9701276..9735465hg38UCSC Ensembl
Outerchr10:9700776..9735965hg38UCSC Ensembl
chr10:9743239..9777428hg19UCSC Ensembl
Innerchr10:9743239..9777428hg19UCSC Ensembl
Outerchr10:9742739..9777928hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3834190
hg1934190
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622316
Supporting Variants
SamplesHG03049
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13694188
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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