A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239556



Internal ID20806596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43124474..43125025hg38UCSC Ensembl
chr15:43416672..43417223hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38552
hg19552
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594172
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239556
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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