A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919674



Internal ID22694896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142415664..142795703hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38380040
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1925n209
Supporting Variantsnssv17430295
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919674
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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