A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5960833



Internal ID22735792
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 Variantsnssv17413325
Samples
Known GenesFGF1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5960833
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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