A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17079784



Internal ID21437470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40037615..40037698hg38UCSC Ensembl
chr15:40329816..40329899hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591974
Supporting Variants
SamplesHG00731
Known GenesSRP14
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17079784
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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