A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5574371



Internal ID21522786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71347366..71347624hg38UCSC Ensembl
chr3:71396517..71396775hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38259
hg19259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17122904
SamplesNA19650
Known GenesFOXP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5574371
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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