A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15496287



Internal ID5498103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:61638941..61644346hg38UCSC Ensembl
Innerchr16:61638941..61644346hg38UCSC Ensembl
Outerchr16:61638738..61644562hg38UCSC Ensembl
chr16:61672845..61678250hg19UCSC Ensembl
Innerchr16:61672845..61678250hg19UCSC Ensembl
Outerchr16:61672642..61678466hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg385406
hg195406
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638781
Supporting Variants
SamplesHG01060
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15496287
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