A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5564839



Internal ID21513147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140493467..140502704hg38UCSC Ensembl
chr7:140193267..140202504hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg389238
hg199238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17153703
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5564839
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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