A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17459185



Internal ID22517068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:125158055..125162828hg38UCSC Ensembl
chr12:125642601..125647374hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg384774
hg194774
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5858990
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17459185
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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