A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15106682



Internal ID6630674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98475041..98574455hg38UCSC Ensembl
chr14:98941378..99040792hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3899415
hg1999415
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635464
Supporting Variants
SamplesNA20792
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15106682
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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