A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17579646



Internal ID21771689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93327758..93332032hg38UCSC Ensembl
chr11:93060924..93065198hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg384275
hg194275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6021272
Supporting Variants
Samples
Known GenesCCDC67
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17579646
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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