A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238046



Internal ID20805086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:48272544..48272933hg38UCSC Ensembl
chr15:48564741..48565130hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38390
hg19390
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594113
Supporting Variants
Samples
Known GenesSLC12A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238046
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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