A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643236



Internal ID7030005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:77992308..77996724hg38UCSC Ensembl
Innerchr18:77992321..77996712hg38UCSC Ensembl
Outerchr18:77992296..77996737hg38UCSC Ensembl
chr18:75704264..75708680hg19UCSC Ensembl
Innerchr18:75704277..75708668hg19UCSC Ensembl
Outerchr18:75704252..75708693hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg384417
hg194417
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15948745, essv15948744, essv15948748, essv15948747, essv15948749, essv15948751, essv15948746, essv15948750
SamplesHG04096, NA21114, HG03785, HG03861, HG04063, HG03866, HG04026, NA21090
Known GenesLINC01029
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643236
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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