A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13706128



Internal ID3707944
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622471
Supporting Variants
SamplesHG02185
Known GenesPTER
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13706128
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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