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nsv5448655

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,149

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 101 SVs from 18 studies. See in: genome view    
Submitted genomic209,868,912-209,871,060Question Mark
Overlapping variant regions from other studies: 101 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):210,733,636-210,735,784Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5448655Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2209,868,912209,871,060
nsv5448655RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2210,733,636210,735,784

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16924808deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16924808Submitted genomicNC_000002.12:g.209
868912_209871060de
l
GRCh38 (hg38)NC_000002.12Chr2209,868,912209,871,060
nssv16924808RemappedPerfectNC_000002.11:g.210
733636_210735784de
l
GRCh37.p13First PassNC_000002.11Chr2210,733,636210,735,784

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)
nssv16924808<0.00136404
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