A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16291790



Internal ID20501008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25988553..25988553hg38UCSC Ensembl
chr4:25990175..25990175hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38461
hg19461
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758804
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16291790
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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