A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006317



Internal ID21915660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37285809..37286502hg38UCSC Ensembl
chr6:37253585..37254278hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38694
hg19694
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576359
Samples
Known GenesTBC1D22B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006317
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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