A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009841



Internal ID21919184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37224424..37224511hg38UCSC Ensembl
chr6:37192200..37192287hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17569075
Samples
Known GenesTMEM217
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009841
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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