A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765932



Internal ID20541792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36645309..36645309hg38UCSC Ensembl
chr9:36645306..36645306hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38286
hg19286
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294080
Samples
Known GenesMELK
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765932
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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