A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14460139



Internal ID22143824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:39473588..39822325hg38UCSC Ensembl
chr9:41618606..41967343hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38348738
hg19348738
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3548997
Supporting Variants
SamplesHG00514
Known GenesKGFLP2, MGC21881
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14460139
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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