A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547393



Internal ID20920594
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 StatusM
Merged Variants
Supporting Variantsnssv18263231
Samples
Known GenesCAPN7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547393
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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