A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5621408



Internal ID21569713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25924047..25924047hg38UCSC Ensembl
chr4:25925669..25925669hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17128512
SamplesHG00171
Known GenesSMIM20
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5621408
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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