A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909361



Internal ID22684571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:27777601..27777693hg38UCSC Ensembl
chr10:28066530..28066622hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367031
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909361
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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