A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17706433



Internal ID130099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4250208..4251566hg38UCSC Ensembl
chr16:4300209..4301567hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381359
hg191359
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5518601
Supporting Variants
Samples
Known GenesLOC100507501
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17706433
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.003438


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