A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5583563



Internal ID21532090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103452475..103456140hg38UCSC Ensembl
chr7:103092922..103096587hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg383666
hg193666
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17151055
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5583563
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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