A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6030464



Internal ID21939807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8818099..8979570hg38UCSC Ensembl
chr11:8839646..9001117hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38161472
hg19161472
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594068
Samples
Known GenesAKIP1, ASCL3, C11orf16, ST5, TMEM9B, TMEM9B-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6030464
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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