A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14959361



Internal ID1380639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:32862554..32878608hg38UCSC Ensembl
chr14:33331760..33347814hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3816055
hg1916055
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633993
Supporting Variants
SamplesHG01250
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14959361
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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