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nsv6138060

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:112,588

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 386 SVs from 45 studies. See in: genome view    
Submitted genomic153,470,000-153,582,587Question Mark
Overlapping variant regions from other studies: 397 SVs from 46 studies. See in: genome view    
Remapped(Score: Perfect):153,442,476-153,555,063Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6138060Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1153,470,000153,582,587
nsv6138060RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1153,442,476153,555,063

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16890353duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16890353Submitted genomicNC_000001.11:g.153
470000_153582587du
p
GRCh38 (hg38)NC_000001.11Chr1153,470,000153,582,587
nssv16890353RemappedPerfectNC_000001.10:g.153
442476_153555063du
p
GRCh37.p13First PassNC_000001.10Chr1153,442,476153,555,063

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)
nssv16890353<0.00116404
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