A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17457122



Internal ID22515003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79484435..79496652hg38UCSC Ensembl
chr10:81244191..81256408hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3812218
hg1912218
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5854336
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17457122
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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