A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972906



Internal ID22747841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125185245..125185245hg38UCSC Ensembl
chr10:126873814..126873814hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366010
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972906
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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