A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14326795



Internal ID22274676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25027412..25033666hg38UCSC Ensembl
chr6:25027640..25033894hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg386255
hg196255
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3197235
Supporting Variants
SamplesNA19239
Known GenesFAM65B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14326795
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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