A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327302



Internal ID20860439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235086472..235091722hg38UCSC Ensembl
chr1:235249787..235255037hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg385251
hg195251
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202410
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327302
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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