A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897244



Internal ID22672344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158242589..158242675hg38UCSC Ensembl
chr3:157960378..157960464hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426135
Samples
Known GenesRSRC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897244
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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