A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637921



Internal ID21586226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:142656218..142656218hg38UCSC Ensembl
chr5:142035783..142035783hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38287
hg19287
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120766
SamplesNA18939
Known GenesFGF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637921
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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