A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050536



Internal ID21959769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:229157372..229157372hg38UCSC Ensembl
chr1:229293119..229293119hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17532302
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050536
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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