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nsv5466146

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:75

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 127 SVs from 26 studies. See in: genome view    
Submitted genomic110,874,507-110,874,581Question Mark
Overlapping variant regions from other studies: 127 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):111,195,710-111,195,784Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5466146Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6110,874,507110,874,581
nsv5466146RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6111,195,710111,195,784

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16988705duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16988705Submitted genomicNC_000006.12:g.110
874507_110874581du
p
GRCh38 (hg38)NC_000006.12Chr6110,874,507110,874,581
nssv16988705RemappedPerfectNC_000006.11:g.111
195710_111195784du
p
GRCh37.p13First PassNC_000006.11Chr6111,195,710111,195,784

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)
nssv169887050.00196404
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