A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239216



Internal ID20806257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20438070..20589783hg38UCSC Ensembl
chr16:20449392..20601105hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38151714
hg19151714
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583118
Supporting Variants
Samples
Known GenesACSM2A, ACSM2B, ACSM5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239216
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00019


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