A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756988



Internal ID20532848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74894135..74894135hg38UCSC Ensembl
chr15:75186476..75186476hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16281063
Samples
Known GenesMPI
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756988
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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