A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17095614



Internal ID21475253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15773473..15785818hg38UCSC Ensembl
chr17:15676787..15689132hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3812346
hg1912346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588117
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17095614
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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