A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321970



Internal ID20855079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:208401152..208429186hg38UCSC Ensembl
chr1:208574497..208602531hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3828035
hg1928035
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199904
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321970
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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