A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6059382



Internal ID9036785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63336193..63337279hg38UCSC Ensembl
chr18:61003426..61004512hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg381087
hg191087
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2671992
Supporting Variants
SamplesNA19313
Known GenesKDSR
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6059382
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