A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14366681



Internal ID22203656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:52301049..52301318hg38UCSC Ensembl
chr1:52766721..52766990hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3191513
Supporting Variants
SamplesHG00732
Known GenesZFYVE9
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14366681
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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