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nsv5429727

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,221

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 135 SVs from 29 studies. See in: genome view    
Submitted genomic44,311,303-44,312,523Question Mark
Overlapping variant regions from other studies: 135 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):44,776,975-44,778,195Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5429727Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr144,311,30344,312,523
nsv5429727RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr144,776,97544,778,195

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16902560deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16902560Submitted genomicNC_000001.11:g.443
11303_44312523del
GRCh38 (hg38)NC_000001.11Chr144,311,30344,312,523
nssv16902560RemappedPerfectNC_000001.10:g.447
76975_44778195del
GRCh37.p13First PassNC_000001.10Chr144,776,97544,778,195

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)
nssv16902560<0.00126404
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