A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638412



Internal ID7025198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31824710..31830614hg38UCSC Ensembl
Innerchr16:31824710..31830614hg38UCSC Ensembl
Outerchr16:31824664..31830686hg38UCSC Ensembl
chr16:31836031..31841935hg19UCSC Ensembl
Innerchr16:31836031..31841935hg19UCSC Ensembl
Outerchr16:31835985..31842007hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg385905
hg195905
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15441901
SamplesNA06989
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638412
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