A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17438536



Internal ID22496406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:95916855..95917178hg38UCSC Ensembl
chr6:96364731..96365054hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5978494
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17438536
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer