A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104967



Internal ID22014201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130186143..130187437hg38UCSC Ensembl
chr10:131984407..131985701hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg381295
hg191295
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17589532
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104967
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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