A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16000635



Internal ID1961456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15646813..15666335hg38UCSC Ensembl
Innerchr19:15646820..15666328hg38UCSC Ensembl
Outerchr19:15646806..15666342hg38UCSC Ensembl
chr19:15757623..15777145hg19UCSC Ensembl
Innerchr19:15757630..15777138hg19UCSC Ensembl
Outerchr19:15757616..15777152hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3819523
hg1919523
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643775
Supporting Variants
SamplesHG01813
Known GenesCYP4F3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16000635
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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