A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848657



Internal ID22623592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110118166..110120265hg38UCSC Ensembl
chr12:110555971..110558070hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455092
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848657
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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