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nsv5463607

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,378

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 106 SVs from 27 studies. See in: genome view    
Submitted genomic145,823,348-145,827,725Question Mark
Overlapping variant regions from other studies: 106 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):146,144,484-146,148,861Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5463607Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6145,823,348145,827,725
nsv5463607RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6146,144,484146,148,861

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16989558deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16989558Submitted genomicNC_000006.12:g.145
823348_145827725de
l
GRCh38 (hg38)NC_000006.12Chr6145,823,348145,827,725
nssv16989558RemappedPerfectNC_000006.11:g.146
144484_146148861de
l
GRCh37.p13First PassNC_000006.11Chr6146,144,484146,148,861

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)
nssv16989558<0.00156404
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