A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17062774



Internal ID21488909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206864617..206864617hg38UCSC Ensembl
chr1:207037962..207037962hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5621844
Supporting Variants
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17062774
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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