A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4758292



Internal ID20534152
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 StatusM
Merged Variants
Supporting Variantsnssv16280007
Samples
Known GenesCCDC84
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4758292
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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