A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224857



Internal ID20791897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:29399665..29401097hg38UCSC Ensembl
chr12:29552598..29554030hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg381433
hg191433
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588972
Supporting Variants
Samples
Known GenesOVCH1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224857
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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