A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17062409



Internal ID21457516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:201140579..201140579hg38UCSC Ensembl
chr1:201109707..201109707hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38497
hg19497
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5608580
Supporting Variants
SamplesHG02587
Known GenesTMEM9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17062409
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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