A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855831



Internal ID22630766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:119929727..119939657hg38UCSC Ensembl
chr12:120367531..120377461hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg389931
hg199931
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17449862
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855831
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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