A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15967856



Internal ID4969284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:572192..582084hg38UCSC Ensembl
chr19:572192..582084hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg389893
hg199893
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643354
Supporting Variants
SamplesNA12873
Known GenesBSG
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15967856
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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