A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915685



Internal ID22690903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25720214..25723574hg38UCSC Ensembl
chr12:25873148..25876508hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg383361
hg193361
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352654
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915685
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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