A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238985



Internal ID20806025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42196023..42247614hg38UCSC Ensembl
chr15:42488221..42539812hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3851592
hg1951592
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587307
Supporting Variants
Samples
Known GenesMIR627, TMEM87A, VPS39
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238985
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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