A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14995426



Internal ID3914878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:43268367..43380167hg38UCSC Ensembl
chr14:43737570..43849370hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38111801
hg19111801
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3634272
Supporting Variants
SamplesHG03567
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14995426
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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