A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15060886



Internal ID3819622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73881793..73882949hg38UCSC Ensembl
Innerchr14:73881833..73882910hg38UCSC Ensembl
Outerchr14:73881754..73882989hg38UCSC Ensembl
chr14:74348496..74349652hg19UCSC Ensembl
Innerchr14:74348536..74349613hg19UCSC Ensembl
Outerchr14:74348457..74349692hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381157
hg191157
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3634922
Supporting Variants
SamplesHG03458
Known GenesPTGR2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15060886
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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