A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17478816



Internal ID22536718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:4775181..4790868hg38UCSC Ensembl
chr17:4678476..4694163hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3815688
hg1915688
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5878783
Supporting Variants
Samples
Known GenesGLTPD2, TM4SF5, VMO1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17478816
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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