A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759945



Internal ID20535805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95658503..95658503hg38UCSC Ensembl
chr5:94994207..94994207hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264793
Samples
Known GenesSPATA9
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759945
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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