A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17085551



Internal ID21434870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3656330..3656385hg38UCSC Ensembl
chr16:3706331..3706386hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5600585
Supporting Variants
SamplesHG00731
Known GenesDNASE1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17085551
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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