A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16283141



Internal ID20492359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:45482662..45482759hg38UCSC Ensembl
chr12:45876445..45876542hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736826
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16283141
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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