A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660467



Internal ID9579886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85006839..85009573hg38UCSC Ensembl
chr16:85040445..85043179hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg382735
hg192735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5799864, essv5995077, essv6560132, essv6301312, essv5574988
SamplesNA18861, NA18916, NA19383, NA19900, NA18487
Known GenesZDHHC7
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660467
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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