A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5945142



Internal ID22720616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62391367..62393178hg38UCSC Ensembl
chr15:62683566..62685377hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg381812
hg191812
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372131
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5945142
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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