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nsv5877280

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:77,598

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 359 SVs from 57 studies. See in: genome view    
Submitted genomic192,579,422-192,657,019Question Mark
Overlapping variant regions from other studies: 359 SVs from 57 studies. See in: genome view    
Remapped(Score: Perfect):192,548,552-192,626,149Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5877280Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1192,579,422192,657,019
nsv5877280RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1192,548,552192,626,149

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17364281duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17364281Submitted genomicNC_000001.11:g.192
579422_192657019du
p
GRCh38 (hg38)NC_000001.11Chr1192,579,422192,657,019
nssv17364281RemappedPerfectNC_000001.10:g.192
548552_192626149du
p
GRCh37.p13First PassNC_000001.10Chr1192,548,552192,626,149

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv173642810.00111820
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