A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5954905



Internal ID22730131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141703339..141703339hg38UCSC Ensembl
chr7:141403139..141403139hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17443148
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5954905
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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