A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17472148



Internal ID22530040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58480332..58493436hg38UCSC Ensembl
chr16:58514236..58527340hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3813105
hg1913105
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5884195
Supporting Variants
Samples
Known GenesNDRG4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17472148
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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