A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17383964



Internal ID22441834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69829074..69834100hg38UCSC Ensembl
chr15:70121413..70126439hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg385027
hg195027
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5974131
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17383964
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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