A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5582858



Internal ID21531375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106835232..106835460hg38UCSC Ensembl
chr7:106475677..106475905hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38229
hg19229
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17143234
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5582858
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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