A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528766



Internal ID22398157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138171024..138171397hg38UCSC Ensembl
chr6:138492161..138492534hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38374
hg19374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14330312, nssv14330313
SamplesNA19239, NA19240
Known GenesKIAA1244
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528766
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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