A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403641



Internal ID21061194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:169832229..169839497hg38UCSC Ensembl
chr5:169259233..169266501hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg387269
hg197269
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216391
Samples
Known GenesDOCK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403641
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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