A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464982



Internal ID22522870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:91109630..91114129hg38UCSC Ensembl
chr12:91503407..91507906hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg384500
hg194500
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5858920
Supporting Variants
Samples
Known GenesLUM
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17464982
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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