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nsv5526551

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:118

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 132 SVs from 25 studies. See in: genome view    
Submitted genomic39,428,039-39,428,156Question Mark
Overlapping variant regions from other studies: 130 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):37,584,292-37,584,409Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5526551Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1739,428,03939,428,156
nsv5526551RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1737,584,29237,584,409

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17713044deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17713044Submitted genomicNC_000017.11:g.394
28039_39428156del
GRCh38 (hg38)NC_000017.11Chr1739,428,03939,428,156
nssv17713044RemappedPerfectNC_000017.10:g.375
84292_37584409del
GRCh37.p13First PassNC_000017.10Chr1737,584,29237,584,409

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)
nssv17713044<0.00156404
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