A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352423



Internal ID22578092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:111504944..111504944hg38UCSC Ensembl
chr10:113264702..113264702hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5959167
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352423
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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