A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15080054



Internal ID6176355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:81665068..81708684hg38UCSC Ensembl
chr14:82131412..82175028hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3843617
hg1943617
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635093
Supporting Variants
SamplesNA19713
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15080054
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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