A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643199



Internal ID7029968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76942794..76965241hg38UCSC Ensembl
Innerchr18:76942944..76965091hg38UCSC Ensembl
Outerchr18:76942644..76965391hg38UCSC Ensembl
chr18:74654750..74677197hg19UCSC Ensembl
Innerchr18:74654900..74677047hg19UCSC Ensembl
Outerchr18:74654600..74677347hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3822448
hg1922448
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15943888, essv15943887
SamplesNA06984, HG03061
Known GenesZNF236
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643199
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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