A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5600646



Internal ID21549287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:13501228..13501333hg38UCSC Ensembl
chr17:13404545..13404650hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17093572
SamplesNA19238
Known GenesHS3ST3A1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5600646
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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