A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642230



Internal ID6682311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36471217..36473814hg38UCSC Ensembl
Innerchr18:36471217..36473814hg38UCSC Ensembl
Outerchr18:36471030..36473968hg38UCSC Ensembl
chr18:34051180..34053777hg19UCSC Ensembl
Innerchr18:34051180..34053777hg19UCSC Ensembl
Outerchr18:34050993..34053931hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg382598
hg192598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15842452
SamplesNA18916
Known GenesFHOD3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642230
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