A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851395



Internal ID22626330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:3876965..3881864hg38UCSC Ensembl
chr12:3986131..3991030hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg384900
hg194900
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462564
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851395
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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