A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6143621



Internal ID342822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:127004476..127004540hg38UCSC Ensembl
chr11:126874371..126874435hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17051527
Samples
Known GenesKIRREL3-AS3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6143621
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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