A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5579697



Internal ID21528178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37124301..37124357hg38UCSC Ensembl
chr4:37125923..37125979hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17123601
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5579697
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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