A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644853



Internal ID6684916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55856144..55856663hg38UCSC Ensembl
Innerchr19:55856194..55856614hg38UCSC Ensembl
Outerchr19:55856095..55856713hg38UCSC Ensembl
chr19:56367510..56368029hg19UCSC Ensembl
Innerchr19:56367560..56367980hg19UCSC Ensembl
Outerchr19:56367461..56368079hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38520
hg19520
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16100750
SamplesHG02067
Known GenesNLRP4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644853
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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