A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921978



Internal ID22697202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163489424..163489664hg38UCSC Ensembl
chr6:163910456..163910696hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412842
Samples
Known GenesQKI
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921978
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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