A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17062967



Internal ID21469552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:217914494..217914494hg38UCSC Ensembl
chr1:218087836..218087836hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5618072
Supporting Variants
SamplesHG03125
Known GenesLINC00210
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17062967
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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