A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15371913



Internal ID5373729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8681250..8681899hg38UCSC Ensembl
Innerchr16:8681262..8681888hg38UCSC Ensembl
Outerchr16:8681239..8681911hg38UCSC Ensembl
chr16:8775107..8775756hg19UCSC Ensembl
Innerchr16:8775119..8775745hg19UCSC Ensembl
Outerchr16:8775096..8775768hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38650
hg19650
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637839
Supporting Variants
SamplesHG00110
Known GenesABAT
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15371913
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