A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851708



Internal ID22626643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:91148048..91151784hg38UCSC Ensembl
chr12:91541825..91545561hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg383737
hg193737
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465096, nssv17462010
Samples
Known GenesDCN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851708
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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