A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5576967



Internal ID21525413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1829041..1829220hg38UCSC Ensembl
chr4:1830768..1830947hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17133290
SamplesNA18534
Known GenesLETM1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5576967
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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