A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17087958



Internal ID21478759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1457326..1458293hg38UCSC Ensembl
chr17:1360620..1361587hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38968
hg19968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5599834
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17087958
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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