A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5959024



Internal ID22734069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25883218..25883218hg38UCSC Ensembl
chr7:25922838..25922838hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444711
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5959024
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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