A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287769



Internal ID20496987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150135392..150135392hg38UCSC Ensembl
chr3:149853179..149853179hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4751634
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287769
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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