A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18241087



Internal ID20808127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55811747..55813069hg38UCSC Ensembl
chr15:56103945..56105267hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg381323
hg191323
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585963
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18241087
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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