A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292674



Internal ID20501892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:56978489..56978489hg38UCSC Ensembl
chr4:57844655..57844655hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4757408
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292674
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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