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nsv6300383

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:16,840,437

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 44515 SVs from 133 studies. See in: genome view    
Remapped(Score: Perfect):26,833,978-43,674,414Question Mark
Overlapping variant regions from other studies: 44518 SVs from 133 studies. See in: genome view    
Submitted genomic26,834,087-43,674,516Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6300383RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr526,833,97843,674,414
nsv6300383Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000005.9Chr526,834,08743,674,516

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17666471duplicationCuratedCurated

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17666471RemappedPerfectNC_000005.10:g.268
33978_43674414dup		GRCh38.p12First PassNC_000005.10Chr526,833,97843,674,414
nssv17666471Submitted genomicNC_000005.9:g.2683
4087_43674516dup		GRCh37 (hg19)NC_000005.9Chr526,834,08743,674,516

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv176664710.0573666404
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