A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17366872



Internal ID22592541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128826785..128826785hg38UCSC Ensembl
chr10:130625049..130625049hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5979895
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17366872
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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