A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331005



Internal ID20864165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244263411..244263463hg38UCSC Ensembl
chr1:244426713..244426765hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200656
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331005
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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