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nsv4259796

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:126

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 22 SVs from 7 studies. See in: genome view    
Remapped(Score: Perfect):48,601,162-48,601,287Question Mark
Overlapping variant regions from other studies: 20 SVs from 7 studies. See in: genome view    
Submitted genomic46,678,524-46,678,649Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4259796RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1748,601,16248,601,287
nsv4259796Submitted genomicGRCh37.p13Primary AssemblyNC_000017.10Chr1746,678,52446,678,649

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15957971duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15957971RemappedPerfectNC_000017.11:g.486
01162_48601287dup
GRCh38.p12First PassNC_000017.11Chr1748,601,16248,601,287
nssv15957971Submitted genomicNC_000017.10:g.466
78524_46678649dup
GRCh37.p13NC_000017.10Chr1746,678,52446,678,649

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)
nssv159579710.01327621348
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