A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5571309



Internal ID9725180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:85277634..85280956hg38UCSC Ensembl
Outerchr16:85277597..85281006hg38UCSC Ensembl
Innerchr16:85311240..85314562hg19UCSC Ensembl
Outerchr16:85311203..85314612hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg383410
hg193410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668928
Supporting Variants
SamplesNA19625
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5571309
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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