A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943096



Internal ID22718540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36569591..36569670hg38UCSC Ensembl
chr15:36861792..36861871hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17371281
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943096
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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