A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330553



Internal ID20863710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158991501..159004900hg38UCSC Ensembl
chr1:158961291..158974690hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3813400
hg1913400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv398n223
Supporting Variantsnssv18200960
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330553
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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