A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16043933



Internal ID6044494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34296741..34419464hg38UCSC Ensembl
Innerchr19:34296774..34419431hg38UCSC Ensembl
Outerchr19:34296708..34419497hg38UCSC Ensembl
chr19:34787646..34910369hg19UCSC Ensembl
Innerchr19:34787679..34910336hg19UCSC Ensembl
Outerchr19:34787613..34910402hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38122724
hg19122724
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644206
Supporting Variants
SamplesHG02760
Known GenesGPI, KIAA0355, PDCD2L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16043933
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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