A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5620801



Internal ID21569106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:219080589..219080589hg38UCSC Ensembl
chr2:219945311..219945311hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17111452
SamplesHG02011
Known GenesNHEJ1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5620801
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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