A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101220



Internal ID22010453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:167156342..167520155hg38UCSC Ensembl
chr3:166874130..167237943hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38363814
hg19363814
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537830
Samples
Known GenesSERPINI2, WDR49, ZBBX
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101220
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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