A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637915



Internal ID7024703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10797963..10799305hg38UCSC Ensembl
Innerchr16:10798015..10799253hg38UCSC Ensembl
Outerchr16:10797911..10799357hg38UCSC Ensembl
chr16:10891820..10893162hg19UCSC Ensembl
Innerchr16:10891872..10893110hg19UCSC Ensembl
Outerchr16:10891768..10893214hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg381343
hg191343
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15374051
SamplesNA20518
Known GenesTVP23A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637915
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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