A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14440325



Internal ID22236876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99838928..99838928hg38UCSC Ensembl
chr10:101598685..101598685hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3547599
Supporting Variants
SamplesHG00733
Known GenesABCC2
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)nssv14440325
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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