A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17477130



Internal ID22535030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11877050..11879999hg38UCSC Ensembl
chr18:11877049..11879998hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg382950
hg192950
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5874687
Supporting Variants
Samples
Known GenesGNAL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17477130
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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