A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16291877



Internal ID20501095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:149995272..149995272hg38UCSC Ensembl
chr4:150916424..150916424hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4764687
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16291877
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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