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nsv6289788

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 140 SVs from 21 studies. See in: genome view    
Submitted genomic80,700,460-80,700,460Question Mark
Overlapping variant regions from other studies: 140 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):78,674,260-78,674,260Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6289788Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1780,700,46080,700,460
nsv6289788RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1778,674,26078,674,260

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17922193insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17922193Submitted genomicNC_000017.11:g.807
00460_80700461ins5
7
GRCh38 (hg38)NC_000017.11Chr1780,700,46080,700,460
nssv17922193RemappedPerfectNC_000017.10:g.786
74260_78674261ins5
7
GRCh37.p13First PassNC_000017.10Chr1778,674,26078,674,260

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)
nssv17922193<0.00112288
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