A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14447739



Internal ID22243294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:209903537..209903537hg38UCSC Ensembl
chr2:210768261..210768261hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3532200
Supporting Variants
SamplesHG00733
Known GenesUNC80
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsSequences at least 70% masked by tandem repeat finder or contained within a tandem repeat
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14447739
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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