A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6052039



Internal ID21961272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150717515..150717515hg38UCSC Ensembl
chr1:150689991..150689991hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527201
Samples
Known GenesHORMAD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6052039
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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