A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16913869



Internal ID9996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:62285075..62285079hg38UCSC Ensembl
chr2:62512210..62512214hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5553680
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16913869
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000624


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