A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18240199



Internal ID20807239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43857554..43858068hg38UCSC Ensembl
chr15:44149752..44150266hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38515
hg19515
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585796
Supporting Variants
Samples
Known GenesWDR76
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18240199
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00032


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