A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17472783



Internal ID22530675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:72975483..72993507hg38UCSC Ensembl
chr16:73009382..73027406hg19UCSC Ensembl
Cytoband16q22.3
Allele length
AssemblyAllele length
hg3818025
hg1918025
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877826
Supporting Variants
Samples
Known GenesZFHX3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17472783
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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