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nsv5456000

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,214

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 99 SVs from 26 studies. See in: genome view    
Submitted genomic150,228,680-150,234,893Question Mark
Overlapping variant regions from other studies: 99 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):150,549,816-150,556,029Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5456000Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6150,228,680150,234,893
nsv5456000RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6150,549,816150,556,029

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16989689deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16989689Submitted genomicNC_000006.12:g.150
228680_150234893de
l
GRCh38 (hg38)NC_000006.12Chr6150,228,680150,234,893
nssv16989689RemappedPerfectNC_000006.11:g.150
549816_150556029de
l
GRCh37.p13First PassNC_000006.11Chr6150,549,816150,556,029

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)
nssv16989689<0.00126404
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