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nsv4504970

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 50 SVs from 4 studies. See in: genome view    
Remapped(Score: Perfect):37,007,840-37,007,840Question Mark
Overlapping variant regions from other studies: 50 SVs from 4 studies. See in: genome view    
Submitted genomic37,581,977-37,581,977Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4504970RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1337,007,84037,007,840
nsv4504970Submitted genomicGRCh37.p13Primary AssemblyNC_000013.10Chr1337,581,97737,581,977

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16005301alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16005301RemappedPerfectNC_000013.11:g.370
07840_37007841ins2
81
GRCh38.p12First PassNC_000013.11Chr1337,007,84037,007,840
nssv16005301Submitted genomicNC_000013.10:g.375
81977_37581978ins2
81
GRCh37.p13NC_000013.10Chr1337,581,97737,581,977

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)
nssv160053014.6e-005121694
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