A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638640



Internal ID7025425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:52836741..52855078hg38UCSC Ensembl
Innerchr16:52836752..52855068hg38UCSC Ensembl
Outerchr16:52836731..52855089hg38UCSC Ensembl
chr16:52870653..52888990hg19UCSC Ensembl
Innerchr16:52870664..52888980hg19UCSC Ensembl
Outerchr16:52870643..52889001hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3818338
hg1918338
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15478710
SamplesHG01939
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638640
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer