A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17362913



Internal ID22588582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23350791..23350791hg38UCSC Ensembl
chr10:23639720..23639720hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5965701
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17362913
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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