A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5642595



Internal ID21590900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28531173..28531173hg38UCSC Ensembl
chr6:28498950..28498950hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17153805
SamplesNA12329
Known GenesGPX5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5642595
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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