A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525236



Internal ID20898597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4230264..4269121hg38UCSC Ensembl
chr19:4230261..4269118hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3838858
hg1938858
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197431
Samples
Known GenesCCDC94, EBI3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525236
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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