A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16976460



Internal ID51695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161907342..161907342hg38UCSC Ensembl
chr5:161334348..161334348hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5537185
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16976460
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00125


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