A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17061506



Internal ID21432536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:163344641..163344641hg38UCSC Ensembl
chr1:163314431..163314431hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5611318
Supporting Variants
SamplesHG00731
Known GenesNUF2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17061506
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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