A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637822



Internal ID7024610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8131141..8167356hg38UCSC Ensembl
Innerchr16:8131145..8167353hg38UCSC Ensembl
Outerchr16:8131138..8167360hg38UCSC Ensembl
chr16:8181143..8217358hg19UCSC Ensembl
Innerchr16:8181147..8217355hg19UCSC Ensembl
Outerchr16:8181140..8217362hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3836216
hg1936216
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15368181, essv15368182, essv15368183
SamplesHG02383, HG02409, HG01811
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637822
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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