A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5622755



Internal ID21571060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:19877081..19877081hg38UCSC Ensembl
chr2:20076842..20076842hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38440
hg19440
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17111016
SamplesNA20509
Known GenesLINC00954
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5622755
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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