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nsv5435607

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,716

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 95 SVs from 29 studies. See in: genome view    
Submitted genomic44,598,951-44,602,666Question Mark
Overlapping variant regions from other studies: 95 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):44,640,443-44,644,158Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5435607Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr344,598,95144,602,666
nsv5435607RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr344,640,44344,644,158

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16933653deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16933653Submitted genomicNC_000003.12:g.445
98951_44602666del
GRCh38 (hg38)NC_000003.12Chr344,598,95144,602,666
nssv16933653RemappedPerfectNC_000003.11:g.446
40443_44644158del
GRCh37.p13First PassNC_000003.11Chr344,640,44344,644,158

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)
nssv16933653<0.00156404
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