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nsv4864628

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,072

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    
Remapped(Score: Perfect):38,843,709-38,845,916Question Mark
Overlapping variant regions from other studies: 131 SVs from 23 studies. See in: genome view    
Submitted genomic36,999,962-37,002,169Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4864628RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1738,843,764 (-55, +30)38,845,835 (-30, +81)
nsv4864628Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000017.10Chr1737,000,017 (-55, +30)37,002,088 (-30, +81)

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16389230duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16389230RemappedPerfectNC_000017.11:g.(38
843709_38843794)_(
38845805_38845916)
dup
GRCh38.p12First PassNC_000017.11Chr1738,843,764 (-55, +30)38,845,835 (-30, +81)
nssv16389230Submitted genomicNC_000017.10:g.(36
999962_37000047)_(
37002058_37002169)
dup
GRCh37 (hg19)NC_000017.10Chr1737,000,017 (-55, +30)37,002,088 (-30, +81)

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)
nssv16389230<0.001316834
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