A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17060173



Internal ID21483330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:119843100..119843100hg38UCSC Ensembl
chr1:120385723..120385723hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5616097
Supporting Variants
SamplesHG03732
Known GenesNBPF7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17060173
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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