A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013887



Internal ID21923230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45676336..45680278hg38UCSC Ensembl
chr10:46171784..46175726hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg383943
hg193943
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586079
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013887
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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