A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263332



Internal ID20472550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:181624295..181632442hg38UCSC Ensembl
chr4:182545448..182553595hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg388148
hg198148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4732987
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263332
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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