A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644820



Internal ID6684884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54861699..54877213hg38UCSC Ensembl
Innerchr19:54861699..54877213hg38UCSC Ensembl
Outerchr19:54861199..54877713hg38UCSC Ensembl
chr19:55373154..55388669hg19UCSC Ensembl
Innerchr19:55373154..55388669hg19UCSC Ensembl
Outerchr19:55372654..55389169hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3815515
hg1915516
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16100208
SamplesHG03760
Known GenesFCAR, KIR3DL2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644820
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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