A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658959



Internal ID9578378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31515615..31810222hg38UCSC Ensembl
chr16:31526936..31821543hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38294608
hg19294608
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5879719, essv5735760, essv6134158
SamplesNA19703, NA18951, NA19147
Known GenesAHSP, CLUHP3, YBX3P1, ZNF720
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658959
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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