A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331128



Internal ID20864289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:3408605..3408689hg38UCSC Ensembl
chr1:3325169..3325253hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203628
Samples
Known GenesPRDM16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331128
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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