A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5627286



Internal ID21575591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:3454184..3454184hg38UCSC Ensembl
chr5:3454298..3454298hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38228
hg19228
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17133161
SamplesHG03065
Known GenesLINC01019
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5627286
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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