A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16947793



Internal ID32555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:29019151..29019188hg38UCSC Ensembl
chr4:29020773..29020810hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5538929
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16947793
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.010147


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