A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5606231



Internal ID21554536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:174454787..174454787hg38UCSC Ensembl
chr2:175319515..175319515hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38224
hg19224
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17110451
SamplesHG03125
Known GenesGPR155
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5606231
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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