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nsv5016251

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,223

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 133 SVs from 23 studies. See in: genome view    
Submitted genomic38,843,684-38,845,958Question Mark
Overlapping variant regions from other studies: 131 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):36,999,937-37,002,211Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5016251Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1738,843,712 (-28, +45)38,845,934 (-24, +24)
nsv5016251RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1736,999,965 (-28, +45)37,002,187 (-24, +24)

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16566842deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16566842Submitted genomicNC_000017.11:g.(38
843684_38843757)_(
38845910_38845958)
del
GRCh38 (hg38)NC_000017.11Chr1738,843,712 (-28, +45)38,845,934 (-24, +24)
nssv16566842RemappedPerfectNC_000017.10:g.(36
999937_37000010)_(
37002163_37002211)
del
GRCh37.p13First PassNC_000017.10Chr1736,999,965 (-28, +45)37,002,187 (-24, +24)

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv16566842<0.001229246
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