A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17388060



Internal ID22445930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40334160..40334221hg38UCSC Ensembl
chr15:40626361..40626422hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5927814
Supporting Variants
Samples
Known GenesC15orf52
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17388060
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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