A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5951548



Internal ID22726908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107727434..107727434hg38UCSC Ensembl
chr7:107367879..107367879hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38367
hg19367
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17443339
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5951548
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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