A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17091672



Internal ID21462447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:70810648..70811381hg38UCSC Ensembl
chr16:70844551..70845284hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg38734
hg19734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5586712
Supporting Variants
SamplesHG02818
Known GenesHYDIN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17091672
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