A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019536



Internal ID21928879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149387340..149392128hg38UCSC Ensembl
chr7:149084431..149089219hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg384789
hg194789
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563305
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019536
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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