A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5612040



Internal ID21560345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99588899..99588899hg38UCSC Ensembl
chr4:100510056..100510056hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17125455
SamplesHG00731
Known GenesMTTP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5612040
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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