A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860661



Internal ID22635596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:23210186..23212229hg38UCSC Ensembl
chr12:23363120..23365163hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg382044
hg192044
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454368
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860661
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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