A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110992



Internal ID22020225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66567882..66793680hg38UCSC Ensembl
chr7:66032869..66258667hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38225799
hg19225799
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563221
Samples
Known GenesKCTD7, LOC493754, RABGEF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110992
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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