A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643772



Internal ID7030530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15609436..15612298hg38UCSC Ensembl
Innerchr19:15609457..15612277hg38UCSC Ensembl
Outerchr19:15609415..15612319hg38UCSC Ensembl
chr19:15720247..15723109hg19UCSC Ensembl
Innerchr19:15720268..15723088hg19UCSC Ensembl
Outerchr19:15720226..15723130hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg382863
hg192863
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15999982
SamplesHG02390
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643772
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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