A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321554



Internal ID20854661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:200487418..200543358hg38UCSC Ensembl
chr1:200456546..200512486hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3855941
hg1955941
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202346
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321554
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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