A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16271499



Internal ID20480717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:126515457..126515516hg38UCSC Ensembl
chr3:126234300..126234359hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4737633
Supporting Variants
Samples
Known GenesUROC1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16271499
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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