A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17381482



Internal ID22439352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72171325..72175177hg38UCSC Ensembl
chr15:72463666..72467518hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg383853
hg193853
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5967771
Supporting Variants
Samples
Known GenesGRAMD2
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17381482
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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