A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324022



Internal ID20857146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244815441..244816151hg38UCSC Ensembl
chr1:244978743..244979453hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38711
hg19711
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200667
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324022
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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