A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17477154



Internal ID22535055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13778445..13782418hg38UCSC Ensembl
chr18:13778444..13782417hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg383974
hg193974
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5887465
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17477154
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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