A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876890



Internal ID22651852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:7315365..7315463hg38UCSC Ensembl
chr2:7455496..7455594hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17399922
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876890
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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