A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639176



Internal ID7025959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:77851813..77855595hg38UCSC Ensembl
Innerchr16:77851813..77855595hg38UCSC Ensembl
Outerchr16:77851493..77855855hg38UCSC Ensembl
chr16:77885710..77889492hg19UCSC Ensembl
Innerchr16:77885710..77889492hg19UCSC Ensembl
Outerchr16:77885390..77889752hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg383783
hg193783
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15528356, essv15528357, essv15528355
SamplesHG00369, NA19439, NA19376
Known GenesVAT1L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639176
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer