A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925917



Internal ID22701144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132531038..132537590hg38UCSC Ensembl
chr10:134344542..134351094hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg386553
hg196553
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17369264
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925917
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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