A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101417



Internal ID22010650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:124725858..124758132hg38UCSC Ensembl
chr3:124444705..124476979hg19UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg3832275
hg1932275
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17538409
Samples
Known GenesUMPS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101417
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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