A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17373684



Internal ID22599353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92771249..92772757hg38UCSC Ensembl
chr15:93314479..93315987hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381509
hg191509
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5933730
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17373684
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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