A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852955



Internal ID22627890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:105838888..105840951hg38UCSC Ensembl
chr12:106232666..106234729hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg382064
hg192064
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463393
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852955
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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