A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319040



Internal ID20852132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165938286..165953864hg38UCSC Ensembl
chr1:165907523..165923101hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg3815579
hg1915579
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201942
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319040
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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