A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5582191



Internal ID21530702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119408416..119408770hg38UCSC Ensembl
chr4:120329571..120329925hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38355
hg19355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17131832
SamplesHG01505
Known GenesLINC01061
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5582191
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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