A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263231



Internal ID20830271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15221185..15221966hg38UCSC Ensembl
chr3:15262692..15263473hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38782
hg19782
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547393
Supporting Variants
Samples
Known GenesCAPN7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263231
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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