A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17098014



Internal ID21430043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:72685321..72685321hg38UCSC Ensembl
chr17:70681460..70681460hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5650867
Supporting Variants
SamplesHG00731
Known GenesSLC39A11
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17098014
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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