A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326359



Internal ID20859494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25689440..25709343hg38UCSC Ensembl
chr1:26015931..26035834hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3819904
hg1919904
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202845
Samples
Known GenesMAN1C1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326359
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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