A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576302



Internal ID20949373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20421525..20598189hg38UCSC Ensembl
chr16:20432847..20609511hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38176665
hg19176665
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2724n223
Supporting Variantsnssv18239210
Samples
Known GenesACSM2A, ACSM2B, ACSM5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576302
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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