A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17109384



Internal ID21442128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15611606..15611732hg38UCSC Ensembl
chr2:15751730..15751856hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5575298
Supporting Variants
SamplesHG00732
Known GenesDDX1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17109384
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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