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nsv5456741

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:47,752

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 397 SVs from 66 studies. See in: genome view    
Submitted genomic177,021,924-177,069,675Question Mark
Overlapping variant regions from other studies: 397 SVs from 66 studies. See in: genome view    
Remapped(Score: Perfect):176,448,925-176,496,676Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5456741Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5177,021,924177,069,675
nsv5456741RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5176,448,925176,496,676

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16978208duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16978208Submitted genomicNC_000005.10:g.177
021924_177069675du
p
GRCh38 (hg38)NC_000005.10Chr5177,021,924177,069,675
nssv16978208RemappedPerfectNC_000005.9:g.1764
48925_176496676dup
GRCh37.p13First PassNC_000005.9Chr5176,448,925176,496,676

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)
nssv16978208<0.00116404
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