A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866466



Internal ID22641401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:102929511..102930510hg38UCSC Ensembl
chr12:103323289..103324288hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17466206, nssv17458936
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866466
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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