A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14421485



Internal ID22159574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:170716807..170716807hg38UCSC Ensembl
chr2:171573317..171573317hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3858754
hg1958754
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3542729
Supporting Variants
SamplesHG00514
Known GenesSP5
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14421485
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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