A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857265



Internal ID22632200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:64189048..64191547hg38UCSC Ensembl
chr12:64582828..64585327hg19UCSC Ensembl
Cytoband12q14.2
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462307
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857265
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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