A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643644



Internal ID6683715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9923855..9929381hg38UCSC Ensembl
Innerchr19:9923855..9929381hg38UCSC Ensembl
Outerchr19:9923752..9929494hg38UCSC Ensembl
chr19:10034531..10040057hg19UCSC Ensembl
Innerchr19:10034531..10040057hg19UCSC Ensembl
Outerchr19:10034428..10040170hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg385527
hg195527
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15990254
SamplesNA19072
Known GenesOLFM2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643644
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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