A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17707633



Internal ID131299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29808745..29810074hg38UCSC Ensembl
chr16:29820066..29821395hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381330
hg191330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5529260
Supporting Variants
Samples
Known GenesMAZ
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17707633
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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