A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856894



Internal ID22631829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93457770..93460963hg38UCSC Ensembl
chr12:93851546..93854739hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg383194
hg193194
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv441n209
Supporting Variantsnssv17452380
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856894
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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