A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018229



Internal ID21927572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44536209..44537870hg38UCSC Ensembl
chr10:45031657..45033318hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg381662
hg191662
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584720
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018229
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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