A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643836



Internal ID6683905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18307632..18308378hg38UCSC Ensembl
Innerchr19:18307682..18308328hg38UCSC Ensembl
Outerchr19:18307570..18308440hg38UCSC Ensembl
chr19:18418442..18419188hg19UCSC Ensembl
Innerchr19:18418492..18419138hg19UCSC Ensembl
Outerchr19:18418380..18419250hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38747
hg19747
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16003941, essv16003940
SamplesHG03947, HG04035
Known GenesLSM4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643836
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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