A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5566829



Internal ID21515159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42704119..42707419hg38UCSC Ensembl
chr4:42706136..42709436hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg383301
hg193301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17129823
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5566829
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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