A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760000



Internal ID20535860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10685908..10685908hg38UCSC Ensembl
chr2:10826034..10826034hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260769
Samples
Known GenesNOL10
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760000
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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