A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18240577



Internal ID20807617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90572007..90572763hg38UCSC Ensembl
chr15:91115239..91115995hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38757
hg19757
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582074
Supporting Variants
Samples
Known GenesCRTC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18240577
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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