A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766552



Internal ID20542412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16089458..16089458hg38UCSC Ensembl
chr7:16129083..16129083hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290543
Samples
Known GenesISPD
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766552
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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