A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639519



Internal ID7026299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87568563..87573486hg38UCSC Ensembl
Innerchr16:87568606..87573444hg38UCSC Ensembl
Outerchr16:87568521..87573529hg38UCSC Ensembl
chr16:87602169..87607092hg19UCSC Ensembl
Innerchr16:87602212..87607050hg19UCSC Ensembl
Outerchr16:87602127..87607135hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg384924
hg194924
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15555141
SamplesNA19070
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639519
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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