A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622193



Internal ID7009052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4333609..4336912hg38UCSC Ensembl
Innerchr10:4333617..4336905hg38UCSC Ensembl
Outerchr10:4333602..4336920hg38UCSC Ensembl
chr10:4375801..4379104hg19UCSC Ensembl
Innerchr10:4375809..4379097hg19UCSC Ensembl
Outerchr10:4375794..4379112hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg383304
hg193304
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13682795
SamplesHG01817
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622193
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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