A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643587



Internal ID7030346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7503335..7504677hg38UCSC Ensembl
Innerchr19:7503345..7504667hg38UCSC Ensembl
Outerchr19:7503325..7504687hg38UCSC Ensembl
chr19:7568221..7569563hg19UCSC Ensembl
Innerchr19:7568231..7569553hg19UCSC Ensembl
Outerchr19:7568211..7569573hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381343
hg191343
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15987329
SamplesHG03786
Known GenesC19orf45
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643587
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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