A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927129



Internal ID22702357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6382397..6382447hg38UCSC Ensembl
chr10:6424359..6424409hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367658
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927129
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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