nsv5456708

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,393

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 97 SVs from 16 studies. See in: genome view    
Submitted genomic131,033,996-131,038,388Question Mark
Overlapping variant regions from other studies: 97 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):131,355,136-131,359,528Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5456708Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6131,033,996131,038,388
nsv5456708RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6131,355,136131,359,528

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16969445deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16969445Submitted genomicNC_000006.12:g.131
033996_131038388de
l
GRCh38 (hg38)NC_000006.12Chr6131,033,996131,038,388
nssv16969445RemappedPerfectNC_000006.11:g.131
355136_131359528de
l
GRCh37.p13First PassNC_000006.11Chr6131,355,136131,359,528

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)
nssv16969445<0.00116404
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