U.S. flag

An official website of the United States government

nsv5402816

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 158 SVs from 20 studies. See in: genome view    
Submitted genomic37,991,904-37,991,955Question Mark
Overlapping variant regions from other studies: 158 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):38,219,047-38,219,098Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5402816Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr237,991,90437,991,955
nsv5402816RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr238,219,04738,219,098

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16911851alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16911851Submitted genomicNC_000002.12:g.379
91904_37991955ins2
81
GRCh38 (hg38)NC_000002.12Chr237,991,90437,991,955
nssv16911851RemappedPerfectNC_000002.11:g.382
19047_38219098ins2
81
GRCh37.p13First PassNC_000002.11Chr238,219,04738,219,098

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)
nssv16911851<0.00126404
Support Center