A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17576184



Internal ID21768227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:118296861..118301297hg38UCSC Ensembl
chr6:118618024..118622460hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg384437
hg194437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6016421
Supporting Variants
Samples
Known GenesSLC35F1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17576184
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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