A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280007



Internal ID20489225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119009442..119009442hg38UCSC Ensembl
chr11:118880152..118880152hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758292
Supporting Variants
Samples
Known GenesCCDC84
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280007
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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