A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5955792



Internal ID22730990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23560143..23560143hg38UCSC Ensembl
chr10:23849072..23849072hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351348
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5955792
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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