A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329200



Internal ID20862351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32124034..32125979hg38UCSC Ensembl
chr1:32589635..32591580hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg381946
hg191946
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203596
Samples
Known GenesKPNA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329200
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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