A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5623419



Internal ID21571724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:216885189..216885189hg38UCSC Ensembl
chr1:217058531..217058531hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38417
hg19417
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17062946
SamplesHG03125
Known GenesESRRG
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5623419
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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