A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760366



Internal ID20536226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156671656..156671656hg38UCSC Ensembl
chr7:156464350..156464350hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292505
Samples
Known GenesRNF32
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760366
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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