A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15355150



Internal ID5356966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:204376..215336hg38UCSC Ensembl
Innerchr16:204376..215336hg38UCSC Ensembl
Outerchr16:203876..215836hg38UCSC Ensembl
chr16:254375..265335hg19UCSC Ensembl
Innerchr16:254375..265335hg19UCSC Ensembl
Outerchr16:253875..265835hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3810961
hg1910961
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637556
Supporting Variants
SamplesNA19786
Known GenesLUC7L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15355150
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