A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755950



Internal ID20531810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:94464234..94464234hg38UCSC Ensembl
chr15:95007463..95007463hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274032
Samples
Known GenesMCTP2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755950
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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