A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5971418



Internal ID22746353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123068641..123068641hg38UCSC Ensembl
chr10:124828157..124828157hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357289
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5971418
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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