A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17084236



Internal ID21447652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56397703..56397768hg38UCSC Ensembl
chr16:56431615..56431680hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5603777
Supporting Variants
SamplesHG00732
Known GenesAMFR
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17084236
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer