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nsv4064879

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,792

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 33 SVs from 8 studies. See in: genome view    
Remapped(Score: Perfect):159,430,609-159,439,400Question Mark
Overlapping variant regions from other studies: 33 SVs from 8 studies. See in: genome view    
Submitted genomic159,400,399-159,409,190Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4064879RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1159,430,609159,439,400
nsv4064879Submitted genomicGRCh37.p13Primary AssemblyNC_000001.10Chr1159,400,399159,409,190

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15962752duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15962752RemappedPerfectNC_000001.11:g.159
430609_159439400du
p
GRCh38.p12First PassNC_000001.11Chr1159,430,609159,439,400
nssv15962752Submitted genomicNC_000001.10:g.159
400399_159409190du
p
GRCh37.p13NC_000001.10Chr1159,400,399159,409,190

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)
nssv159627524.6e-005121694
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