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nsv5500519

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15,978

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 176 SVs from 43 studies. See in: genome view    
Submitted genomic49,281,704-49,297,681Question Mark
Overlapping variant regions from other studies: 176 SVs from 43 studies. See in: genome view    
Remapped(Score: Perfect):49,675,487-49,691,464Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5500519Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1249,281,70449,297,681
nsv5500519RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1249,675,48749,691,464

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17058265duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17058265Submitted genomicNC_000012.12:g.492
81704_49297681dup
GRCh38 (hg38)NC_000012.12Chr1249,281,70449,297,681
nssv17058265RemappedPerfectNC_000012.11:g.496
75487_49691464dup
GRCh37.p13First PassNC_000012.11Chr1249,675,48749,691,464

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)
nssv170582650.004246404
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