A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591448



Internal ID20964519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50444857..50445739hg38UCSC Ensembl
chr15:50737054..50737936hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38883
hg19883
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238106
Samples
Known GenesUSP8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591448
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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