A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100751



Internal ID22009984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:79402908..80175540hg38UCSC Ensembl
chr6:80112625..80885257hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38772633
hg19772633
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559107
Samples
Known GenesBCKDHB, C6orf7, ELOVL4, LCA5, RNY4, SH3BGRL2, TTK
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100751
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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