A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16271300



Internal ID20480518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:111651270..111651344hg38UCSC Ensembl
chr12:112089074..112089148hg19UCSC Ensembl
Cytoband12q24.12
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4742207
Supporting Variants
Samples
Known GenesBRAP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16271300
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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