A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17089847



Internal ID21407461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85208798..85208897hg38UCSC Ensembl
chr16:85242404..85242503hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5601835
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17089847
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