A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14413606



Internal ID22148923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45497645..45497645hg38UCSC Ensembl
chr1:45963317..45963317hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38428
hg19428
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3539961
Supporting Variants
SamplesHG00514
Known GenesCCDC163P
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)nssv14413606
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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