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nsv5543230

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:41

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 118 SVs from 28 studies. See in: genome view    
Submitted genomic103,097,390-103,097,430Question Mark
Overlapping variant regions from other studies: 118 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):102,737,837-102,737,877Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5543230Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7103,097,390103,097,430
nsv5543230RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7102,737,837102,737,877

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17000554insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17000554Submitted genomicNC_000007.14:g.103
097390_103097430in
s57
GRCh38 (hg38)NC_000007.14Chr7103,097,390103,097,430
nssv17000554RemappedPerfectNC_000007.13:g.102
737837_102737877in
s57
GRCh37.p13First PassNC_000007.13Chr7102,737,837102,737,877

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)
nssv17000554<0.00116404
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