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nsv5461492

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:161

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 113 SVs from 21 studies. See in: genome view    
Submitted genomic102,579,188-102,579,348Question Mark
Overlapping variant regions from other studies: 113 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):103,500,345-103,500,505Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5461492Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4102,579,188102,579,348
nsv5461492RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4103,500,345103,500,505

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16953445deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16953445Submitted genomicNC_000004.12:g.102
579188_102579348de
l
GRCh38 (hg38)NC_000004.12Chr4102,579,188102,579,348
nssv16953445RemappedPerfectNC_000004.11:g.103
500345_103500505de
l
GRCh37.p13First PassNC_000004.11Chr4103,500,345103,500,505

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)
nssv16953445<0.00116404
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