A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529337



Internal ID22398729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24878884..24879196hg38UCSC Ensembl
chr6:24879112..24879424hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14326792, nssv14326793, nssv14326791, nssv14326790, nssv14326794, nssv14326789
SamplesHG00512, NA19238, NA19239, HG00732, NA19240, HG00514
Known GenesFAM65B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529337
Frequency
Sample Size9
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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