A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17383235



Internal ID22441105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4297977..4302884hg38UCSC Ensembl
chr16:4347978..4352885hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg384908
hg194908
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5934564
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17383235
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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