A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14357604



Internal ID22284059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33311924..33311975hg38UCSC Ensembl
chr11:33333470..33333521hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3225652
Supporting Variants
SamplesNA19239
Known GenesHIPK3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14357604
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