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nsv5841449

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,066

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 693 SVs from 79 studies. See in: genome view    
Submitted genomic140,850,106-140,859,171Question Mark
Overlapping variant regions from other studies: 688 SVs from 78 studies. See in: genome view    
Remapped(Score: Perfect):140,229,691-140,238,756Question Mark
Overlapping variant regions from other studies: 312 SVs from 37 studies. See in: genome view    
Remapped(Score: Perfect):85,282-94,347Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5841449Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5140,850,106140,859,171
nsv5841449RemappedPerfectGRCh37.p13Primary AssemblySecond PassNC_000005.9Chr5140,229,691140,238,756
nsv5841449RemappedPerfectGRCh37.p13PATCHESFirst PassNW_004775428.1Chr5|NW_00
4775428.1
85,28294,347

Variant Call Information

Variant Call IDTypeMethodAnalysisCopy number
nssv17495598copy number variationSequencingSequence alignment0
nssv17495599copy number variationSequencingSequence alignment2

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv17495598Submitted genomicGRCh38 (hg38)NC_000005.10Chr5140,850,106140,859,171
nssv17495599Submitted genomicGRCh38 (hg38)NC_000005.10Chr5140,850,106140,859,171
nssv17495598RemappedPerfectGRCh37.p13First PassNW_004775428.1Chr5|NW_00
4775428.1
85,28294,347
nssv17495599RemappedPerfectGRCh37.p13First PassNW_004775428.1Chr5|NW_00
4775428.1
85,28294,347
nssv17495598RemappedPerfectGRCh37.p13Second PassNC_000005.9Chr5140,229,691140,238,756
nssv17495599RemappedPerfectGRCh37.p13Second PassNC_000005.9Chr5140,229,691140,238,756

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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