A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17454302



Internal ID22512178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45852411..45865210hg38UCSC Ensembl
chr10:46347859..46360658hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3812800
hg1912800
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860075
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17454302
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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