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nsv4255369

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:382,640

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 409 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):74,388,518-74,771,157Question Mark
Overlapping variant regions from other studies: 409 SVs from 20 studies. See in: genome view    
Submitted genomic72,384,657-72,767,296Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4255369RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1774,388,51874,771,157
nsv4255369Submitted genomicGRCh37.p13Primary AssemblyNC_000017.10Chr1772,384,65772,767,296

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15958300duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15958300RemappedPerfectNC_000017.11:g.743
88518_74771157dup
GRCh38.p12First PassNC_000017.11Chr1774,388,51874,771,157
nssv15958300Submitted genomicNC_000017.10:g.723
84657_72767296dup
GRCh37.p13NC_000017.10Chr1772,384,65772,767,296

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)
nssv159583004.6e-005121694
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