A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17479018



Internal ID22536920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58489024..58491773hg38UCSC Ensembl
chr16:58522928..58525677hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg382750
hg192750
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5875313
Supporting Variants
Samples
Known GenesNDRG4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17479018
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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