A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759315



Internal ID20535175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:8063973..8063973hg38UCSC Ensembl
chr2:8204103..8204103hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294373
Samples
Known GenesLINC00299
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759315
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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