A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864511



Internal ID22639446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142773250..142774865hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381616
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1929n209
Supporting Variantsnssv17502151, nssv17504532
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864511
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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