A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320919



Internal ID20854020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:166565693..166566200hg38UCSC Ensembl
chr1:166534930..166535437hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg38508
hg19508
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201957
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320919
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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