A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5641005



Internal ID21589310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93928116..93928116hg38UCSC Ensembl
chr7:93557428..93557428hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17147830
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5641005
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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