A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866997



Internal ID22641932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:130875206..130876448hg38UCSC Ensembl
chr12:131359751..131360993hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg381243
hg191243
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv466n209
Supporting Variantsnssv17449849, nssv17464984
Samples
Known GenesRAN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866997
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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