A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16915474



Internal ID11056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:73643309..73703619hg38UCSC Ensembl
chr2:73870436..73930746hg19UCSC Ensembl
Cytoband2p13.1
Allele length
AssemblyAllele length
hg3860311
hg1960311
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5443922
Supporting Variants
Samples
Known GenesALMS1P, NAT8B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16915474
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003748


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