A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220900



Internal ID20787940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:97813083..99306980hg38UCSC Ensembl
chr12:98206861..99700758hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg381493898
hg191493898
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590693
Supporting Variants
Samples
Known GenesANKS1B, APAF1, IKBIP, LOC643770, MIR4303, SLC25A3, SLC9A7P1, SNORA53, TMPO, TMPO-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220900
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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