A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763276



Internal ID20539136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:31938666..31938666hg38UCSC Ensembl
chr7:31978279..31978279hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272439
Samples
Known GenesPDE1C
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763276
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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