A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18015626



Internal ID20582666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102109453..102118445hg38UCSC Ensembl
chr14:102575790..102584782hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg388993
hg198993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500760
Supporting Variants
Samples
Known GenesHSP90AA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18015626
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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