A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3548997



Internal ID22417944
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14456672, nssv14462648, nssv14456145, nssv14461139, nssv14457682, nssv14454358, nssv14453767, nssv14460139
SamplesNA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesKGFLP2, MGC21881
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3548997
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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