A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16976277



Internal ID51582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:147183590..147183640hg38UCSC Ensembl
chr5:146563153..146563203hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5539892
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16976277
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.004371


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