A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029149



Internal ID21938492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:60770464..60770557hg38UCSC Ensembl
chr16:60804368..60804461hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17630742
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029149
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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