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nsv5393599

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,714

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 188 SVs from 51 studies. See in: genome view    
Remapped(Score: Perfect):70,201,084-70,203,797Question Mark
Overlapping variant regions from other studies: 188 SVs from 51 studies. See in: genome view    
Submitted genomic70,594,864-70,597,577Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5393599RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1270,201,08470,203,797
nsv5393599Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000012.11Chr1270,594,86470,597,577

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16887935sva deletionCuratedCurated

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16887935RemappedPerfectNC_000012.12:g.702
01084_70203797del
GRCh38.p12First PassNC_000012.12Chr1270,201,08470,203,797
nssv16887935Submitted genomicNC_000012.11:g.705
94864_70597577del
GRCh37 (hg19)NC_000012.11Chr1270,594,86470,597,577

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)
nssv168879350.6892013429222
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