U.S. flag

An official website of the United States government

nsv5415815

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,583

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 254 SVs from 31 studies. See in: genome view    
Submitted genomic65,623,043-65,624,625Question Mark
Overlapping variant regions from other studies: 254 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):64,842,922-64,844,504Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5415815Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX65,623,04365,624,625
nsv5415815RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX64,842,92264,844,504

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17740402deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17740402Submitted genomicNC_000023.11:g.656
23043_65624625del
GRCh38 (hg38)NC_000023.11ChrX65,623,04365,624,625
nssv17740402RemappedPerfectNC_000023.10:g.648
42922_64844504del
GRCh37.p13First PassNC_000023.10ChrX64,842,92264,844,504

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)
nssv177404020.013826404
Support Center