A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849267



Internal ID22624202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:38554944..38559932hg38UCSC Ensembl
chr12:38948746..38953734hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg384989
hg194989
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455664
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849267
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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