A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv611e214



Internal ID20122034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:31380933..31436217hg38UCSC Ensembl
chr18:28960896..29016180hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3855285
hg1955285
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3642124, esv3642123
SamplesHG00864, HG02072
Known GenesDSG4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv611e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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