A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367471



Internal ID21025024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14946001..14949400hg38UCSC Ensembl
chr3:14987508..14990907hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg383400
hg193400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211403
Samples
Known GenesFGD5-AS1, NR2C2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367471
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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