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nsv5003456

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,330

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 641 SVs from 53 studies. See in: genome view    
Submitted genomic30,017,721-30,019,051Question Mark
Overlapping variant regions from other studies: 641 SVs from 53 studies. See in: genome view    
Remapped(Score: Perfect):30,029,042-30,030,372Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5003456Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1630,017,72130,019,050 (-1, +1)
nsv5003456RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1630,029,04230,030,371 (-1, +1)

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16560372deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16560372Submitted genomicNC_000016.10:g.300
17721_(30019049_30
019051)del
GRCh38 (hg38)NC_000016.10Chr1630,017,72130,019,050 (-1, +1)
nssv16560372RemappedPerfectNC_000016.9:g.3002
9042_(30030370_300
30372)del
GRCh37.p13First PassNC_000016.9Chr1630,029,04230,030,371 (-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)
nssv16560372<0.001629246
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