A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915522



Internal ID22690740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162928503..163095764hg38UCSC Ensembl
chr6:163349535..163516796hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38167262
hg19167262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425675
Samples
Known GenesPACRG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915522
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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