A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011661



Internal ID21921004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:86706877..86721946hg38UCSC Ensembl
chr5:86002694..86017763hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3815070
hg1915070
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555957
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011661
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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