U.S. flag

An official website of the United States government

nsv5453639

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:35,179,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 99239 SVs from 143 studies. See in: genome view    
Submitted genomic163,047,000-198,226,000Question Mark
Overlapping variant regions from other studies: 99243 SVs from 143 studies. See in: genome view    
Remapped(Score: Good):162,764,788-197,952,871Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5453639Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3163,047,000198,226,000
nsv5453639RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3162,764,788197,952,871

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16940252duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16940252Submitted genomicNC_000003.12:g.163
047000_198226000du
p
GRCh38 (hg38)NC_000003.12Chr3163,047,000198,226,000
nssv16940252RemappedGoodNC_000003.11:g.162
764788_197952871du
p
GRCh37.p13First PassNC_000003.11Chr3162,764,788197,952,871

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)
nssv16940252<0.00116404
Support Center