A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17062635



Internal ID21413145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:209887942..209887942hg38UCSC Ensembl
chr1:210061287..210061287hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5619500
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17062635
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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