A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17095209



Internal ID21484149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58074261..58074437hg38UCSC Ensembl
chr17:56151622..56151798hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5602316
Supporting Variants
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17095209
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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