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nsv6144051

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:133,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1429 SVs from 94 studies. See in: genome view    
Submitted genomic11,002,000-11,135,000Question Mark
Overlapping variant regions from other studies: 1430 SVs from 94 studies. See in: genome view    
Remapped(Score: Perfect):11,154,599-11,287,599Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6144051Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1211,002,00011,135,000
nsv6144051RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1211,154,59911,287,599

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17053086duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17053086Submitted genomicNC_000012.12:g.110
02000_11135000dup
GRCh38 (hg38)NC_000012.12Chr1211,002,00011,135,000
nssv17053086RemappedPerfectNC_000012.11:g.111
54599_11287599dup
GRCh37.p13First PassNC_000012.11Chr1211,154,59911,287,599

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)
nssv17053086<0.00156390
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