A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17104500



Internal ID21512782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36159810..36322017hg38UCSC Ensembl
chr19:36650712..36812919hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38162208
hg19162208
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5668787
Supporting Variants
Samples
Known GenesLINC00665, LOC100134317, ZNF146, ZNF565
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17104500
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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