A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17375113



Internal ID22600782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26052191..26053775hg38UCSC Ensembl
chr15:26297338..26298922hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg381585
hg191585
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5928942
Supporting Variants
Samples
Known GenesLOC100128714
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17375113
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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