A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644552



Internal ID7031307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:47346533..47348066hg38UCSC Ensembl
Innerchr19:47346569..47348031hg38UCSC Ensembl
Outerchr19:47346498..47348102hg38UCSC Ensembl
chr19:47849790..47851323hg19UCSC Ensembl
Innerchr19:47849826..47851288hg19UCSC Ensembl
Outerchr19:47849755..47851359hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg381534
hg191534
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16071051
SamplesHG01942
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644552
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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