A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15109105



Internal ID5110921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101801418..101961003hg38UCSC Ensembl
chr14:102267755..102427340hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38159586
hg19159586
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635536
Supporting Variants
SamplesHG03971
Known GenesPPP2R5C
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15109105
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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