A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14331032



Internal ID22193798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132600767..132601153hg38UCSC Ensembl
chr6:132921906..132922292hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3192408
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14331032
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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