A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14329948



Internal ID22234423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:61027382..61137247hg38UCSC Ensembl
chr6:57995129..58087659hg19UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg38109866
hg1992531
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3244139
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14329948
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer