A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272439



Internal ID20481657
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 StatusS
Merged Variantsnsv4763276
Supporting Variants
Samples
Known GenesPDE1C
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272439
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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