A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15986094



Internal ID5987910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6342431..6353681hg38UCSC Ensembl
Innerchr19:6342931..6353181hg38UCSC Ensembl
Outerchr19:6341431..6354681hg38UCSC Ensembl
chr19:6342442..6353692hg19UCSC Ensembl
Innerchr19:6342942..6353192hg19UCSC Ensembl
Outerchr19:6341442..6354692hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3811251
hg1911251
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643552
Supporting Variants
SamplesHG03740
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15986094
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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