A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18240178



Internal ID20807218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:80990892..80991522hg38UCSC Ensembl
chr16:81024497..81025127hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg38631
hg19631
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588324
Supporting Variants
Samples
Known GenesCMC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18240178
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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