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nsv4320566

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:34,432,790

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 23200 SVs from 25 studies. See in: genome view    
Remapped(Score: Good):114,947,405-149,380,194Question Mark
Overlapping variant regions from other studies: 23191 SVs from 25 studies. See in: genome view    
Submitted genomic114,283,102-148,759,757Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4320566RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr5114,947,405149,380,194
nsv4320566Submitted genomicGRCh37.p13Primary AssemblyNC_000005.9Chr5114,283,102148,759,757

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16091366inversionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16091366RemappedGoodNC_000005.10:g.114
947405_149380194in
v
GRCh38.p12First PassNC_000005.10Chr5114,947,405149,380,194
nssv16091366Submitted genomicNC_000005.9:g.1142
83102_148759757inv
GRCh37.p13NC_000005.9Chr5114,283,102148,759,757

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv160913664.6e-005121694
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