A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413593



Internal ID21071146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:44178285..44185029hg38UCSC Ensembl
chr6:44146022..44152766hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg386745
hg196745
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18144067
Samples
Known GenesCAPN11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413593
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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