A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5574041



Internal ID21522452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1573028..1573094hg38UCSC Ensembl
chr4:1574755..1574821hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17129313
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5574041
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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