A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5569172



Internal ID21517527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23589996..23591419hg38UCSC Ensembl
chr7:23629615..23631038hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg381424
hg191424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17152351
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5569172
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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