A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14421505



Internal ID22159606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:178757206..178757206hg38UCSC Ensembl
chr2:179621933..179621933hg19UCSC Ensembl
Cytoband2q31.2
Allele length
AssemblyAllele length
hg38468
hg19468
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3536665
Supporting Variants
SamplesHG00514
Known GenesTTN
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)nssv14421505
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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