A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323788



Internal ID20856910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16888501..16898100hg38UCSC Ensembl
chr1:17214996..17224595hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg389600
hg199600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201617
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323788
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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