A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331290



Internal ID20864453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:166404298..166411523hg38UCSC Ensembl
chr1:166373535..166380760hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg387226
hg197226
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201954
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331290
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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