A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17126482



Internal ID21497432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87807395..87807395hg38UCSC Ensembl
chr4:88728547..88728547hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5609136
Supporting Variants
SamplesNA19238
Known GenesIBSP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17126482
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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