A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329272



Internal ID20862423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168423666..168437351hg38UCSC Ensembl
chr1:168392904..168406589hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3813686
hg1913686
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201539
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329272
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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