A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16269669



Internal ID20478887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:137060301..137063459hg38UCSC Ensembl
chr3:136779143..136782301hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg383159
hg193159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4737477
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16269669
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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