A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17094259



Internal ID21450195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:13782608..13782673hg38UCSC Ensembl
chr17:13685925..13685990hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5598453
Supporting Variants
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17094259
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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