A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17706013



Internal ID129679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56397743..56398118hg38UCSC Ensembl
chr16:56431655..56432030hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38376
hg19376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6144842
Supporting Variants
Samples
Known GenesAMFR
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17706013
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.383666


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