A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637991



Internal ID7024777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:13766133..13767909hg38UCSC Ensembl
Innerchr16:13766133..13767909hg38UCSC Ensembl
Outerchr16:13765964..13768000hg38UCSC Ensembl
chr16:13859990..13861766hg19UCSC Ensembl
Innerchr16:13859990..13861766hg19UCSC Ensembl
Outerchr16:13859821..13861857hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg381777
hg191777
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15378591
SamplesHG02611
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637991
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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