A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317260



Internal ID20850344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:191784901..191804400hg38UCSC Ensembl
chr1:191754031..191773530hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg3819500
hg1919500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199823
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317260
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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