A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17061013



Internal ID21439697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:159888493..159888493hg38UCSC Ensembl
chr1:159858283..159858283hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5621004
Supporting Variants
SamplesHG00732
Known GenesCCDC19
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17061013
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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