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nsv5423223

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:573,083

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1305 SVs from 71 studies. See in: genome view    
Submitted genomic89,283,835-89,856,917Question Mark
Overlapping variant regions from other studies: 1295 SVs from 71 studies. See in: genome view    
Remapped(Score: Good):89,749,518-90,322,476Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5423223Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr189,283,83589,856,917
nsv5423223RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr189,749,51890,322,476

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16905601duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16905601Submitted genomicNC_000001.11:g.892
83835_89856917dup
GRCh38 (hg38)NC_000001.11Chr189,283,83589,856,917
nssv16905601RemappedGoodNC_000001.10:g.897
49518_90322476dup
GRCh37.p13First PassNC_000001.10Chr189,749,51890,322,476

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)
nssv16905601<0.00126404
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