A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050125



Internal ID21959358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:234544600..234544600hg38UCSC Ensembl
chr2:235453244..235453244hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17536854
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050125
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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