A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866088



Internal ID22641023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66543435..66549863hg38UCSC Ensembl
chr7:66008422..66014850hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg386429
hg196429
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17508868
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866088
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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