A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17563221



Internal ID21887576
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 StatusS
Merged Variantsnsv6110992
Supporting Variants
Samples
Known GenesKCTD7, LOC493754, RABGEF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17563221
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer