A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3556728



Internal ID22425549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62420001..62487139hg38UCSC Ensembl
chr9:46731302..46798440hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3867139
hg1967139
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14456921, nssv14455232, nssv14456957, nssv14462030, nssv14466627, nssv14453301, nssv14460406, nssv14459483, nssv14454203
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesKGFLP1
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3556728
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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