A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924977



Internal ID22700204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140642364..140643993hg38UCSC Ensembl
chr7:140342164..140343793hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381630
hg191630
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447708
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924977
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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