A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325576



Internal ID20858707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:239187344..239401897hg38UCSC Ensembl
chr1:239350644..239565197hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38214554
hg19214554
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202522
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325576
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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