A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853668



Internal ID22628603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:56643122..56645356hg38UCSC Ensembl
chr12:57036906..57039140hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg382235
hg192235
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459480
Samples
Known GenesATP5B, SNORD59A, SNORD59B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853668
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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