A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886833



Internal ID22661822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95781632..95802608hg38UCSC Ensembl
chr15:96324861..96345837hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3820977
hg1920977
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474956
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886833
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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