A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15492709



Internal ID3184023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:59622654..59625816hg38UCSC Ensembl
Innerchr16:59622804..59625666hg38UCSC Ensembl
Outerchr16:59622504..59625966hg38UCSC Ensembl
chr16:59656558..59659720hg19UCSC Ensembl
Innerchr16:59656708..59659570hg19UCSC Ensembl
Outerchr16:59656408..59659870hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg383163
hg193163
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638750
Supporting Variants
SamplesHG02799
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15492709
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