A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622316



Internal ID7009175
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13694188
SamplesHG03049
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622316
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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