A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334923



Internal ID20868112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23520080..23534616hg38UCSC Ensembl
chr1:23846572..23861108hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3814537
hg1914537
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202416
Samples
Known GenesE2F2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334923
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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