A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17091509



Internal ID21484541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:13796494..13796635hg38UCSC Ensembl
chr17:13699811..13699952hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588795
Supporting Variants
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17091509
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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