nsv5388923

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:281

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 146 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):80,482,346-80,482,626Question Mark
Overlapping variant regions from other studies: 146 SVs from 32 studies. See in: genome view    
Submitted genomic82,242,102-82,242,382Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5388923RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr1080,482,34680,482,626
nsv5388923Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000010.10Chr1082,242,10282,242,382

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16886322deletionCuratedCurated

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16886322RemappedPerfectNC_000010.11:g.804
82346_80482626del
GRCh38.p12First PassNC_000010.11Chr1080,482,34680,482,626
nssv16886322Submitted genomicNC_000010.10:g.822
42102_82242382del
GRCh37 (hg19)NC_000010.10Chr1082,242,10282,242,382

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)
nssv168863220.027302
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