A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6017441



Internal ID21926784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25863556..25863632hg38UCSC Ensembl
chr6:25863784..25863860hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574055
Samples
Known GenesSLC17A3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6017441
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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