A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14388568



Internal ID22325490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15149439..15149439hg38UCSC Ensembl
chr10:15191438..15191438hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38525
hg19525
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3548678
Supporting Variants
SamplesNA19240
Known GenesNMT2
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)nssv14388568
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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