A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5574779



Internal ID21523199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:52636099..52636230hg38UCSC Ensembl
chr1:53101771..53101902hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17065603
SamplesHG00513
Known GenesFAM159A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5574779
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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