A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17375863



Internal ID22601532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43495064..43495370hg38UCSC Ensembl
chr15:43787262..43787568hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5935186
Supporting Variants
Samples
Known GenesRNU6-28P, TP53BP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17375863
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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