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nsv5454685

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,036

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 178 SVs from 36 studies. See in: genome view    
Submitted genomic17,691,529-17,693,663Question Mark
Overlapping variant regions from other studies: 178 SVs from 36 studies. See in: genome view    
Remapped(Score: Perfect):17,691,760-17,693,894Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5454685Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr617,691,579 (-50, +268)17,693,614 (-247, +49)
nsv5454685RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr617,691,810 (-50, +268)17,693,845 (-247, +49)

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16979224deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16979224Submitted genomicNC_000006.12:g.(17
691529_17691847)_(
17693367_17693663)
del
GRCh38 (hg38)NC_000006.12Chr617,691,579 (-50, +268)17,693,614 (-247, +49)
nssv16979224RemappedPerfectNC_000006.11:g.(17
691760_17692078)_(
17693598_17693894)
del
GRCh37.p13First PassNC_000006.11Chr617,691,810 (-50, +268)17,693,845 (-247, +49)

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)
nssv16979224<0.00126404
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