A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622467



Internal ID7009326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16335820..16352840hg38UCSC Ensembl
Innerchr10:16336320..16352340hg38UCSC Ensembl
Outerchr10:16334820..16353840hg38UCSC Ensembl
chr10:16377819..16394839hg19UCSC Ensembl
Innerchr10:16378319..16394339hg19UCSC Ensembl
Outerchr10:16376819..16395839hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3817021
hg1917021
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13706119, essv13706118
SamplesHG01170, HG01191
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622467
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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