A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17386309



Internal ID22444179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26162620..26163857hg38UCSC Ensembl
chr15:26407767..26409004hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg381238
hg191238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5942898
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17386309
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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