A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059705



Internal ID21968938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:238439268..238439268hg38UCSC Ensembl
chr2:239347909..239347909hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527621
Samples
Known GenesASB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059705
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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