A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5583445



Internal ID21531970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57127301..57127358hg38UCSC Ensembl
chr3:57161329..57161386hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124030
SamplesNA19238
Known GenesIL17RD
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5583445
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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