A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14355444



Internal ID22127860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26016737..26021167hg38UCSC Ensembl
chr1:26343228..26347658hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg384431
hg194431
Variant TypeCNV duplication
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3201331
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14355444
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