A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968192



Internal ID22743127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:91409319..91409319hg38UCSC Ensembl
chr15:91952549..91952549hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38433
hg19433
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17377118
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968192
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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