A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319399



Internal ID20852493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25072461..25099780hg38UCSC Ensembl
chr1:25398952..25426271hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3827320
hg1927320
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202823
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319399
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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