A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17123137



Internal ID21479065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:142596308..142596443hg38UCSC Ensembl
chr5:141975873..141976008hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5569314
Supporting Variants
SamplesHG03486
Known GenesFGF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17123137
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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