A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861783



Internal ID22636718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:21826106..21828481hg38UCSC Ensembl
chr12:21979040..21981415hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg382376
hg192376
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463121
Samples
Known GenesABCC9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861783
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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