A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281063



Internal ID20490281
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 StatusS
Merged Variantsnsv4756988
Supporting Variants
Samples
Known GenesMPI
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281063
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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