A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5582818



Internal ID21531334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2748610..2748745hg38UCSC Ensembl
chr4:2750337..2750472hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17137255
SamplesHG03125
Known GenesTNIP2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5582818
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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