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nsv5503914

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:211

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 118 SVs from 28 studies. See in: genome view    
Submitted genomic34,895,014-34,895,224Question Mark
Overlapping variant regions from other studies: 118 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):35,187,215-35,187,425Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5503914Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1534,895,01434,895,224
nsv5503914RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1535,187,21535,187,425

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17701456deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17701456Submitted genomicNC_000015.10:g.348
95014_34895224del
GRCh38 (hg38)NC_000015.10Chr1534,895,01434,895,224
nssv17701456RemappedPerfectNC_000015.9:g.3518
7215_35187425del
GRCh37.p13First PassNC_000015.9Chr1535,187,21535,187,425

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)
nssv17701456<0.00126404
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