A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14466954



Internal ID22184586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97436188..97461596hg38UCSC Ensembl
chr7:97065500..97090908hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3825409
hg1925409
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3244455
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14466954
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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