A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916783



Internal ID22692002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25383741..25386135hg38UCSC Ensembl
chr7:25423360..25425754hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg382395
hg192395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17438706
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916783
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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