A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292483



Internal ID20501701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:156660556..156660556hg38UCSC Ensembl
chr4:157581708..157581708hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4759692
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292483
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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