A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5575142



Internal ID21523568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185210390..185210441hg38UCSC Ensembl
chr4:186131544..186131595hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17136203
SamplesNA12878
Known GenesSNX25
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5575142
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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