A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907926



Internal ID22683136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25939998..25942927hg38UCSC Ensembl
chr7:25979618..25982547hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg382930
hg192930
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435159
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907926
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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