A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17368119



Internal ID22593788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29789412..29789412hg38UCSC Ensembl
chr10:30078341..30078341hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5959991
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17368119
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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