A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622471



Internal ID6662641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16473422..16476442hg38UCSC Ensembl
Innerchr10:16473447..16476418hg38UCSC Ensembl
Outerchr10:16473398..16476467hg38UCSC Ensembl
chr10:16515421..16518441hg19UCSC Ensembl
Innerchr10:16515446..16518417hg19UCSC Ensembl
Outerchr10:16515397..16518466hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg383021
hg193021
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13706128, essv13706127
SamplesHG02185, HG02134
Known GenesPTER
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622471
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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