A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18241977



Internal ID20809017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75518734..75519234hg38UCSC Ensembl
chr15:75811075..75811575hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586366
Supporting Variants
Samples
Known GenesPTPN9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18241977
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0002


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