A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17089483



Internal ID21510186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5206163..5206357hg38UCSC Ensembl
chr17:5109458..5109652hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588405
Supporting Variants
SamplesNA24385
Known GenesLOC100130950
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17089483
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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