A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397418



Internal ID21054971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:141930776..141939063hg38UCSC Ensembl
chr5:141310341..141318628hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg388288
hg198288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125816
Samples
Known GenesKIAA0141
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397418
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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