A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923868



Internal ID22699095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99306761..99320221hg38UCSC Ensembl
chr7:98904384..98917844hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3813461
hg1913461
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439583
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923868
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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