A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413110



Internal ID21070663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32833888..32837716hg38UCSC Ensembl
chr6:32801665..32805493hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg383829
hg193829
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18142237
Samples
Known GenesTAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413110
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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