A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859195



Internal ID22634130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:2747029..2749387hg38UCSC Ensembl
chr12:2856195..2858553hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg382359
hg192359
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458118
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859195
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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