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nsv5423943

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 143 SVs from 29 studies. See in: genome view    
Submitted genomic63,004,556-63,004,607Question Mark
Overlapping variant regions from other studies: 143 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):61,635,908-61,635,959Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5423943Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2063,004,55663,004,607
nsv5423943RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2061,635,90861,635,959

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17733623alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17733623Submitted genomicNC_000020.11:g.630
04556_63004607ins2
72
GRCh38 (hg38)NC_000020.11Chr2063,004,55663,004,607
nssv17733623RemappedPerfectNC_000020.10:g.616
35908_61635959ins2
72
GRCh37.p13First PassNC_000020.10Chr2061,635,90861,635,959

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)
nssv17733623<0.00126404
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