A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5565317



Internal ID21513629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:36728517..36728832hg38UCSC Ensembl
chr2:36955660..36955975hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17114065
SamplesHG00512
Known GenesVIT
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5565317
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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