A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15815992



Internal ID4498382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:14815740..14838589hg38UCSC Ensembl
chr18:14815739..14838588hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3822850
hg1922850
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3641913
Supporting Variants
SamplesHG03999
Known GenesANKRD30B, MIR3156-2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15815992
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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