A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5623400



Internal ID21571705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57127359..57127359hg38UCSC Ensembl
chr3:57161387..57161387hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17137242
SamplesHG00864
Known GenesIL17RD
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5623400
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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