A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17583264



Internal ID21775307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8818116..8977324hg38UCSC Ensembl
chr11:8839663..8998871hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38159209
hg19159209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6020879
Supporting Variants
Samples
Known GenesAKIP1, ASCL3, C11orf16, ST5, TMEM9B, TMEM9B-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17583264
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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