A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848951



Internal ID22623886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:27980598..27989997hg38UCSC Ensembl
chr12:28133531..28142930hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg389400
hg199400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453590
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848951
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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