A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019101



Internal ID21928444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:123677222..124027180hg38UCSC Ensembl
chr6:123998367..124348325hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38349959
hg19349959
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17560113
Samples
Known GenesNKAIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019101
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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