A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3244455



Internal ID22375865
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14466954, nssv14466184
SamplesHG00731, HG00733
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3244455
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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