A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5964716



Internal ID22739651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99240045..99240045hg38UCSC Ensembl
chr7:98837668..98837668hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447030
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5964716
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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