A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358954



Internal ID21016507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151624156..151634623hg38UCSC Ensembl
chr3:151341944..151352411hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3810468
hg1910468
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209710
Samples
Known GenesMIR548H2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358954
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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