A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847713



Internal ID22622648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:113591072..113592344hg38UCSC Ensembl
chr12:114028877..114030149hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg381273
hg191273
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459786, nssv17467315
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847713
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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