A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5577225



Internal ID21525674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:102318345..102318453hg38UCSC Ensembl
chr2:102934805..102934913hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17107812
SamplesHG03486
Known GenesIL1RL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5577225
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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