A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329888



Internal ID20863041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:59462217..59466258hg38UCSC Ensembl
chr1:59927889..59931930hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg384042
hg194042
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202098
Samples
Known GenesFGGY
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329888
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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