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nsv5543531

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:19

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 110 SVs from 19 studies. See in: genome view    
Submitted genomic25,808,055-25,808,073Question Mark
Overlapping variant regions from other studies: 110 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):26,030,924-26,030,942Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5543531Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr225,808,05525,808,073
nsv5543531RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr226,030,92426,030,942

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16911025insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16911025Submitted genomicNC_000002.12:g.258
08055_25808073ins5
9
GRCh38 (hg38)NC_000002.12Chr225,808,05525,808,073
nssv16911025RemappedPerfectNC_000002.11:g.260
30924_26030942ins5
9
GRCh37.p13First PassNC_000002.11Chr226,030,92426,030,942

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)
nssv16911025<0.00126404
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