A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5605182



Internal ID21553487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31744185..31744185hg38UCSC Ensembl
chr1:32209786..32209786hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg384187
hg194187
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17064719
SamplesHG03065
Known GenesBAI2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5605182
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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