A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358489



Internal ID21016042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158052627..158113670hg38UCSC Ensembl
chr3:157770416..157831459hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3861044
hg1961044
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210371
Samples
Known GenesRSRC1, SHOX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358489
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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