A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3241835



Internal ID22375082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:47613072..47616567hg38UCSC Ensembl
chr7:47652670..47656165hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg383496
hg193496
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14455922, nssv14465459, nssv14461936, nssv14461702
SamplesHG00512, HG00732, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3241835
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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