A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15982232



Internal ID6607015
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643509
Supporting Variants
SamplesNA20774
Known GenesDPP9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15982232
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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