A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15935923



Internal ID4721564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:75863067..75871492hg38UCSC Ensembl
Innerchr18:75863085..75871474hg38UCSC Ensembl
Outerchr18:75863049..75871510hg38UCSC Ensembl
chr18:73575022..73583447hg19UCSC Ensembl
Innerchr18:73575040..73583429hg19UCSC Ensembl
Outerchr18:73575004..73583465hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg388426
hg198426
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643153
Supporting Variants
SamplesNA06984
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15935923
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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