A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5579381



Internal ID21527861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113046429..113046525hg38UCSC Ensembl
chr3:112765276..112765372hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17123167
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5579381
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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