A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639284



Internal ID7026067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:80806600..80852948hg38UCSC Ensembl
Innerchr16:80806620..80852929hg38UCSC Ensembl
Outerchr16:80806581..80852968hg38UCSC Ensembl
chr16:80840497..80886845hg19UCSC Ensembl
Innerchr16:80840517..80886826hg19UCSC Ensembl
Outerchr16:80840478..80886865hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3846349
hg1946349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15534705
SamplesHG02272
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639284
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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