A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5574165



Internal ID21522577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:38755999..38756078hg38UCSC Ensembl
chr2:38983141..38983220hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17113255
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5574165
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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