A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853193



Internal ID22628128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:30794883..30796282hg38UCSC Ensembl
chr12:30947817..30949216hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv358n209
Supporting Variantsnssv17453866, nssv17468063
Samples
Known GenesLINC00941
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853193
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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