A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907712



Internal ID22682922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142313665..142797124hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38483460
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1925n209
Supporting Variantsnssv17442442
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907712
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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