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nsv6148218

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:69

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 118 SVs from 26 studies. See in: genome view    
Submitted genomic119,844,215-119,844,283Question Mark
Overlapping variant regions from other studies: 120 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):120,386,838-120,386,906Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6148218Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1119,844,215119,844,283
nsv6148218RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1120,386,838120,386,906

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17877964deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17877964Submitted genomicNC_000001.11:g.119
844215_119844283de
l
GRCh38 (hg38)NC_000001.11Chr1119,844,215119,844,283
nssv17877964RemappedPerfectNC_000001.10:g.120
386838_120386906de
l
GRCh37.p13First PassNC_000001.10Chr1120,386,838120,386,906

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)
nssv17877964<0.00122342
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