A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324960



Internal ID20858090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:39188704..39199123hg38UCSC Ensembl
chr1:39654376..39664795hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3810420
hg1910420
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203075
Samples
Known GenesMACF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324960
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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