A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17477103



Internal ID22535003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10134616..10145225hg38UCSC Ensembl
chr18:10134613..10145222hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3810610
hg1910610
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5873098
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17477103
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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