A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5940841



Internal ID22716255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40060724..40060809hg38UCSC Ensembl
chr15:40352925..40353010hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17378975
Samples
Known GenesSRP14-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5940841
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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