nsv5474884

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,200

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 208 SVs from 29 studies. See in: genome view    
Submitted genomic127,701,006-127,705,205Question Mark
Overlapping variant regions from other studies: 208 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):128,713,251-128,717,450Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5474884Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8127,701,006127,705,205
nsv5474884RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8128,713,251128,717,450

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17016418deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17016418Submitted genomicNC_000008.11:g.127
701006_127705205de
l
GRCh38 (hg38)NC_000008.11Chr8127,701,006127,705,205
nssv17016418RemappedPerfectNC_000008.10:g.128
713251_128717450de
l
GRCh37.p13First PassNC_000008.10Chr8128,713,251128,717,450

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)
nssv17016418<0.00146404
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