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nsv5432700

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:45

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 129 SVs from 29 studies. See in: genome view    
Submitted genomic36,994,617-36,994,661Question Mark
Overlapping variant regions from other studies: 129 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):37,568,754-37,568,798Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5432700Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1336,994,61736,994,661
nsv5432700RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1337,568,75437,568,798

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17686926alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17686926Submitted genomicNC_000013.11:g.369
94617_36994661ins2
76
GRCh38 (hg38)NC_000013.11Chr1336,994,61736,994,661
nssv17686926RemappedPerfectNC_000013.10:g.375
68754_37568798ins2
76
GRCh37.p13First PassNC_000013.10Chr1337,568,75437,568,798

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)
nssv176869260.0694456404
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