A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639413



Internal ID6679506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84172318..84253359hg38UCSC Ensembl
chr16:84205924..84286965hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3881042
hg1981042
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15545798
SamplesHG03009
Known GenesADAD2, DNAAF1, KCNG4, TAF1C
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639413
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