A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405404



Internal ID21062957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:44157101..44159900hg38UCSC Ensembl
chr6:44124838..44127637hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18144065
Samples
Known GenesCAPN11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405404
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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