A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975047



Internal ID22749982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95232639..95232639hg38UCSC Ensembl
chr15:95775868..95775868hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383805
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975047
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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