A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875102



Internal ID22650057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9810593..9842089hg38UCSC Ensembl
chr2:9950722..9982218hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3831497
hg1931497
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17399493
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875102
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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