A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15997281



Internal ID6938897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14366169..14368823hg38UCSC Ensembl
Innerchr19:14366174..14368818hg38UCSC Ensembl
Outerchr19:14366164..14368828hg38UCSC Ensembl
chr19:14476981..14479635hg19UCSC Ensembl
Innerchr19:14476986..14479630hg19UCSC Ensembl
Outerchr19:14476976..14479640hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg382655
hg192655
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643740
Supporting Variants
SamplesNA21125
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15997281
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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