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nsv4880762

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:67,985,043

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 175509 SVs from 153 studies. See in: genome view    
Remapped(Score: Good):79,688,546-147,673,588Question Mark
Overlapping variant regions from other studies: 175125 SVs from 153 studies. See in: genome view    
Submitted genomic79,317,862-147,370,680Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4880762RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr779,688,546147,673,588
nsv4880762Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr779,317,862147,370,680

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16414225inversionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16414225RemappedGoodNC_000007.14:g.796
88546_147673588inv
GRCh38.p12First PassNC_000007.14Chr779,688,546147,673,588
nssv16414225Submitted genomicNC_000007.13:g.793
17862_147370680inv
GRCh37 (hg19)NC_000007.13Chr779,317,862147,370,680

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)
nssv16414225<0.001116834
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