A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17370385



Internal ID22596054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:48041724..48041822hg38UCSC Ensembl
chr16:48075635..48075733hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5940118
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17370385
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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