A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374554



Internal ID21032107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158503272..158521202hg38UCSC Ensembl
chr3:158221061..158238991hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3817931
hg1917931
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210377
Samples
Known GenesRSRC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374554
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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