A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14331559



Internal ID22282160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111446154..111450479hg38UCSC Ensembl
chr6:111767357..111771682hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg384326
hg194326
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3192943
Supporting Variants
SamplesNA19239
Known GenesREV3L
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14331559
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