A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4431584



Internal ID21393586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78941420..78942249hg38UCSC Ensembl
chr11:78652465..78653294hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38830
hg19830
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15750862
SamplesMDQ010
Known GenesTENM4
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4431584
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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