A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5566356



Internal ID21514681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:46148534..46148959hg38UCSC Ensembl
chr7:46188132..46188557hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg38426
hg19426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17153292
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5566356
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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