A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374849



Internal ID21032402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157882452..157899826hg38UCSC Ensembl
chr3:157600241..157617615hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3817375
hg1917375
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210369
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374849
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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