A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103768



Internal ID22013001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:29209669..29226599hg38UCSC Ensembl
chr5:29209776..29226706hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3816931
hg1916931
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547274
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103768
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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