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nsv5431010

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:395,842

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 983 SVs from 62 studies. See in: genome view    
Submitted genomic98,409,815-98,805,656Question Mark
Overlapping variant regions from other studies: 983 SVs from 62 studies. See in: genome view    
Remapped(Score: Perfect):98,875,371-99,271,212Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5431010Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr198,409,81598,805,656
nsv5431010RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr198,875,37199,271,212

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16906753duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16906753Submitted genomicNC_000001.11:g.984
09815_98805656dup
GRCh38 (hg38)NC_000001.11Chr198,409,81598,805,656
nssv16906753RemappedPerfectNC_000001.10:g.988
75371_99271212dup
GRCh37.p13First PassNC_000001.10Chr198,875,37199,271,212

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)
nssv16906753<0.00116404
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