A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5858514



Internal ID22633449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:30107291..30110000hg38UCSC Ensembl
chr12:30260224..30262933hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg382710
hg192710
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17450567
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5858514
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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