A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760625



Internal ID20536485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73306901..73306901hg38UCSC Ensembl
chr7:72720897..72720897hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295522
Samples
Known GenesNSUN5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760625
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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