A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17476358



Internal ID22534256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1593319..1598242hg38UCSC Ensembl
chr16:1643320..1648243hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg384924
hg194924
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5884036
Supporting Variants
Samples
Known GenesIFT140
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17476358
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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