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nsv6159627

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:286

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 439 SVs from 64 studies. See in: genome view    
Submitted genomic189,846,019-189,846,304Question Mark
Overlapping variant regions from other studies: 439 SVs from 64 studies. See in: genome view    
Remapped(Score: Perfect):190,767,174-190,767,459Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6159627Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4189,846,019189,846,304
nsv6159627RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4190,767,174190,767,459

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17894607deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17894607Submitted genomicNC_000004.12:g.189
846019_189846304de
l
GRCh38 (hg38)NC_000004.12Chr4189,846,019189,846,304
nssv17894607RemappedPerfectNC_000004.11:g.190
767174_190767459de
l
GRCh37.p13First PassNC_000004.11Chr4190,767,174190,767,459

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)
nssv17894607<0.00122134
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