A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17474819



Internal ID22532714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9101978..9107813hg38UCSC Ensembl
chr16:9195835..9201670hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg385836
hg195836
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5882205
Supporting Variants
Samples
Known GenesC16orf72
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17474819
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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