A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16043756



Internal ID4682554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33484468..33485553hg38UCSC Ensembl
Innerchr19:33484499..33485523hg38UCSC Ensembl
Outerchr19:33484438..33485584hg38UCSC Ensembl
chr19:33975374..33976459hg19UCSC Ensembl
Innerchr19:33975405..33976429hg19UCSC Ensembl
Outerchr19:33975344..33976490hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg381086
hg191086
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644189
Supporting Variants
SamplesHG04209
Known GenesPEPD
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16043756
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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