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nsv4330897

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:70,046,808

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 48276 SVs from 26 studies. See in: genome view    
Remapped(Score: Good):89,919,544-159,966,351Question Mark
Overlapping variant regions from other studies: 47803 SVs from 26 studies. See in: genome view    
Submitted genomic90,629,263-160,387,383Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4330897RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr689,919,544159,966,351
nsv4330897Submitted genomicGRCh37.p13Primary AssemblyNC_000006.11Chr690,629,263160,387,383

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16090387inversionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16090387RemappedGoodNC_000006.12:g.899
19544_159966351inv
GRCh38.p12First PassNC_000006.12Chr689,919,544159,966,351
nssv16090387Submitted genomicNC_000006.11:g.906
29263_160387383inv
GRCh37.p13NC_000006.11Chr690,629,263160,387,383

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)
nssv160903874.6e-005121694
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