A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17080101



Internal ID21473814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10729868..10729868hg38UCSC Ensembl
chr17:10633185..10633185hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5652741
Supporting Variants
SamplesHG03371
Known GenesTMEM220, TMEM220-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17080101
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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