A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330607



Internal ID20863765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:162611756..162614382hg38UCSC Ensembl
chr1:162581546..162584172hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg382627
hg192627
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201898
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330607
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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