A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17473360



Internal ID22531253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74658940..74678360hg38UCSC Ensembl
chr16:74692838..74712258hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3819421
hg1919421
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5871203
Supporting Variants
Samples
Known GenesMLKL, RFWD3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17473360
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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