A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15990329



Internal ID5992145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10240829..10242334hg38UCSC Ensembl
Innerchr19:10240880..10242284hg38UCSC Ensembl
Outerchr19:10240779..10242385hg38UCSC Ensembl
chr19:10351505..10353010hg19UCSC Ensembl
Innerchr19:10351556..10352960hg19UCSC Ensembl
Outerchr19:10351455..10353061hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381506
hg191506
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643650
Supporting Variants
SamplesHG04189
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15990329
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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