A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325609



Internal ID20858740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:190466301..190486600hg38UCSC Ensembl
chr1:190435431..190455730hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg3820300
hg1920300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199796
Samples
Known GenesBRINP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325609
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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