A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5650625



Internal ID21598930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:121881808..121881808hg38UCSC Ensembl
chr12:122319714..122319714hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17077637
SamplesHG00731
Known GenesHPD
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5650625
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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