A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929777



Internal ID22705036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:97200088..97201254hg38UCSC Ensembl
chr12:97593866..97595032hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg381167
hg191167
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17368163
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929777
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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