A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320362



Internal ID20853460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:119315792..119334891hg38UCSC Ensembl
chr1:119858415..119877514hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg3819100
hg1919100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200363
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320362
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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