A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15088148



Internal ID6018736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:84785391..84813515hg38UCSC Ensembl
chr14:85251735..85279859hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3828125
hg1928125
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635172
Supporting Variants
SamplesNA19430
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15088148
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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