A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238286



Internal ID20805326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41002834..41003352hg38UCSC Ensembl
chr15:41295032..41295550hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38519
hg19519
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576777
Supporting Variants
Samples
Known GenesINO80
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238286
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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