A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179751



Internal ID20746791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77464100..77687463hg38UCSC Ensembl
chr17:75460182..75683545hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38223364
hg19223364
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528208
Supporting Variants
Samples
Known GenesLOC100507351, SEPT9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179751
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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