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nsv4994558

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:678

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 116 SVs from 25 studies. See in: genome view    
Submitted genomic23,496,226-23,496,906Question Mark
Overlapping variant regions from other studies: 116 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):23,507,547-23,508,227Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4994558Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1623,496,228 (-2, +2)23,496,905 (-1, +1)
nsv4994558RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1623,507,549 (-2, +2)23,508,226 (-1, +1)

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16574276duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16574276Submitted genomicNC_000016.10:g.(23
496226_23496230)_(
23496904_23496906)
dup
GRCh38 (hg38)NC_000016.10Chr1623,496,228 (-2, +2)23,496,905 (-1, +1)
nssv16574276RemappedPerfectNC_000016.9:g.(235
07547_23507551)_(2
3508225_23508227)d
up
GRCh37.p13First PassNC_000016.9Chr1623,507,549 (-2, +2)23,508,226 (-1, +1)

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)
nssv16574276<0.001329246
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