A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18017767



Internal ID20584807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:31658870..31663360hg38UCSC Ensembl
chr14:32128076..32132566hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg384491
hg194491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6491456
Supporting Variants
Samples
Known GenesNUBPL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18017767
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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