A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238938



Internal ID20805978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66347647..66348395hg38UCSC Ensembl
chr15:66639985..66640733hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38749
hg19749
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587888
Supporting Variants
Samples
Known GenesTIPIN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238938
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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