A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199642



Internal ID22349201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3156720..3180156hg38UCSC Ensembl
chr6:3156954..3180390hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3823437
hg1923437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14325891, nssv14325890, nssv14325892
SamplesHG00731, NA19240, HG00514
Known GenesTUBB2A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3199642
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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