A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17452991



Internal ID22510864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79526084..79533089hg38UCSC Ensembl
chr10:81285840..81292845hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg387006
hg197006
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855035
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17452991
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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