A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051766



Internal ID21960999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14623326..14623477hg38UCSC Ensembl
chr21:15995647..15995798hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648697
Samples
Known GenesLOC388813
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051766
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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