A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643505



Internal ID7030264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4572362..4577849hg38UCSC Ensembl
Innerchr19:4572426..4577786hg38UCSC Ensembl
Outerchr19:4572299..4577913hg38UCSC Ensembl
chr19:4572374..4577861hg19UCSC Ensembl
Innerchr19:4572438..4577798hg19UCSC Ensembl
Outerchr19:4572311..4577925hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg385488
hg195488
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15982206
SamplesNA18571
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643505
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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