A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17089096



Internal ID21502095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37380859..37381889hg38UCSC Ensembl
chr17:35737797..35738827hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381031
hg191031
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5587648
Supporting Variants
SamplesNA19239
Known GenesACACA, C17orf78
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17089096
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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