nsv4890946

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,720

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 120 SVs from 25 studies. See in: genome view    
Submitted genomic116,974,588-116,977,308Question Mark
Overlapping variant regions from other studies: 123 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):117,517,210-117,519,930Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4890946Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1116,974,589 (-1, +1)116,977,308 (-1)
nsv4890946RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1117,517,211 (-1, +1)117,519,930 (-1)

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16422734deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16422734Submitted genomicNC_000001.11:g.(11
6974588_116974590)
_(116977307_?)del
GRCh38 (hg38)NC_000001.11Chr1116,974,589 (-1, +1)116,977,308 (-1)
nssv16422734RemappedPerfectNC_000001.10:g.(11
7517210_117517212)
_(117519929_?)del
GRCh37.p13First PassNC_000001.10Chr1117,517,211 (-1, +1)117,519,930 (-1)

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)
nssv16422734<0.001129246
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