A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16291995



Internal ID20501213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:54169919..54169919hg38UCSC Ensembl
chr4:55036086..55036086hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg381420
hg191420
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4755743
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16291995
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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