A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643509



Internal ID7030268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4691715..4694123hg38UCSC Ensembl
Innerchr19:4691715..4694123hg38UCSC Ensembl
Outerchr19:4691461..4694385hg38UCSC Ensembl
chr19:4691727..4694135hg19UCSC Ensembl
Innerchr19:4691727..4694135hg19UCSC Ensembl
Outerchr19:4691473..4694397hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382409
hg192409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15982231, essv15982229, essv15982230, essv15982227, essv15982225, essv15982228, essv15982232, essv15982226
SamplesNA20774, NA19725, HG03908, HG00268, HG01392, HG01182, NA12749, HG01672
Known GenesDPP9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643509
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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