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nsv5505850

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,508,376

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 4310 SVs from 105 studies. See in: genome view    
Submitted genomic86,047,034-87,555,409Question Mark
Overlapping variant regions from other studies: 4300 SVs from 105 studies. See in: genome view    
Remapped(Score: Good):85,758,076-87,266,301Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5505850Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1186,047,03487,555,409
nsv5505850RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1185,758,07687,266,301

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17049625duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17049625Submitted genomicNC_000011.10:g.860
47034_87555409dup
GRCh38 (hg38)NC_000011.10Chr1186,047,03487,555,409
nssv17049625RemappedGoodNC_000011.9:g.8575
8076_87266301dup
GRCh37.p13First PassNC_000011.9Chr1185,758,07687,266,301

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)
nssv17049625<0.00126404
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