A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14331398



Internal ID22194865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:152972827..152972912hg38UCSC Ensembl
chr6:153293962..153294047hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3530058
Supporting Variants
SamplesHG00731
Known GenesFBXO5
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14331398
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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