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nsv4879764

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:83,402,318

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 197825 SVs from 154 studies. See in: genome view    
Remapped(Score: Good):103,800,446-187,202,765Question Mark
Overlapping variant regions from other studies: 197999 SVs from 154 studies. See in: genome view    
Submitted genomic104,416,904-188,067,492Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4879764RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2103,800,448 (-2)187,202,765 (-2)
nsv4879764Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr2104,416,906 (-2)188,067,492 (-2)

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16411123inversionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16411123RemappedGoodNC_000002.12:g.(10
3800446_?)_(187202
763_?)inv
GRCh38.p12First PassNC_000002.12Chr2103,800,448 (-2)187,202,765 (-2)
nssv16411123Submitted genomicNC_000002.11:g.(10
4416904_?)_(188067
490_?)inv
GRCh37 (hg19)NC_000002.11Chr2104,416,906 (-2)188,067,492 (-2)

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)
nssv16411123<0.001116834
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