A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18015631



Internal ID20582671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102156101..102164200hg38UCSC Ensembl
chr14:102622438..102630537hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg388100
hg198100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504193
Supporting Variants
Samples
Known GenesWDR20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18015631
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00104


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