A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17370781



Internal ID22596450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26968283..26968608hg38UCSC Ensembl
chr15:27213430..27213755hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5931803
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17370781
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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