A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848530



Internal ID22623465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122318551..122328220hg38UCSC Ensembl
chr12:122803098..122812767hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg389670
hg199670
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455878
Samples
Known GenesCLIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848530
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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