A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000730



Internal ID21910073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158073422..158073492hg38UCSC Ensembl
chr6:158494454..158494524hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568082
Samples
Known GenesSYNJ2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000730
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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