U.S. flag

An official website of the United States government

nsv5408323

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:39

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 141 SVs from 32 studies. See in: genome view    
Submitted genomic155,146,795-155,146,833Question Mark
Overlapping variant regions from other studies: 148 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):155,119,271-155,119,309Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5408323Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1155,146,795155,146,833
nsv5408323RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1155,119,271155,119,309

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16890433alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16890433Submitted genomicNC_000001.11:g.155
146795_155146833in
s280
GRCh38 (hg38)NC_000001.11Chr1155,146,795155,146,833
nssv16890433RemappedPerfectNC_000001.10:g.155
119271_155119309in
s280
GRCh37.p13First PassNC_000001.10Chr1155,119,271155,119,309

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)
nssv168904330.003196404
Support Center