A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969023



Internal ID22743958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10210789..10210789hg38UCSC Ensembl
chr12:10363388..10363388hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358498
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969023
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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