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nsv6147200

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:11,653

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 89 SVs from 25 studies. See in: genome view    
Submitted genomic26,090,303-26,101,955Question Mark
Overlapping variant regions from other studies: 89 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):26,101,624-26,113,276Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6147200Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1626,090,30326,101,955
nsv6147200RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1626,101,62426,113,276

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17707580mobile element deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17707580Submitted genomicNC_000016.10:g.260
90303_26101955del
GRCh38 (hg38)NC_000016.10Chr1626,090,30326,101,955
nssv17707580RemappedPerfectNC_000016.9:g.2610
1624_26113276del
GRCh37.p13First PassNC_000016.9Chr1626,101,62426,113,276

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)
nssv17707580<0.00126404
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