nsv4754840

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:21,327,858

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 52781 SVs from 127 studies. See in: genome view    
Remapped(Score: Good):103,988,761-125,316,618Question Mark
Overlapping variant regions from other studies: 52770 SVs from 127 studies. See in: genome view    
Submitted genomic104,382,539-125,801,164Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4754840RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr12103,988,761125,316,618
nsv4754840Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000012.11Chr12104,382,539125,801,164

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16259676inversionSequencingSplit read mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16259676RemappedGoodNC_000012.12:g.103
988761_125316618in
v
GRCh38.p12First PassNC_000012.12Chr12103,988,761125,316,618
nssv16259676Submitted genomicNC_000012.11:g.104
382539_125801164in
v
GRCh37 (hg19)NC_000012.11Chr12104,382,539125,801,164

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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