A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920268



Internal ID22695491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:86280768..86367814hg38UCSC Ensembl
chr7:85910084..85997130hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3887047
hg1987047
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448307
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920268
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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