A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16915445



Internal ID11037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:73358651..73358977hg38UCSC Ensembl
chr2:73585779..73586105hg19UCSC Ensembl
Cytoband2p13.1
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5449046
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16915445
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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