A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941033



Internal ID22716450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97691282..97691359hg38UCSC Ensembl
chr15:98234512..98234589hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386274
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941033
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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