A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851132



Internal ID22626067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:4585292..4587370hg38UCSC Ensembl
chr12:4694458..4696536hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg382079
hg192079
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457400
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851132
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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