A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17424908



Internal ID22482778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149477281..149478461hg38UCSC Ensembl
chr5:148856844..148858024hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg381181
hg191181
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5970923
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17424908
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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