A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15528311



Internal ID6777365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:77210206..77215925hg38UCSC Ensembl
Innerchr16:77210233..77215898hg38UCSC Ensembl
Outerchr16:77210179..77215952hg38UCSC Ensembl
chr16:77244103..77249822hg19UCSC Ensembl
Innerchr16:77244130..77249795hg19UCSC Ensembl
Outerchr16:77244076..77249849hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg385720
hg195720
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639164
Supporting Variants
SamplesNA20878
Known GenesSYCE1L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15528311
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