A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18023067



Internal ID20590108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:87925162..87956828hg38UCSC Ensembl
chr14:88391506..88423172hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3831667
hg1931667
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6483899
Supporting Variants
Samples
Known GenesGALC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18023067
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00084


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