U.S. flag

An official website of the United States government

nsv5500265

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:101

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 146 SVs from 25 studies. See in: genome view    
Submitted genomic26,214,137-26,214,237Question Mark
Overlapping variant regions from other studies: 146 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):26,367,070-26,367,170Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5500265Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1226,214,13726,214,237
nsv5500265RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1226,367,07026,367,170

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17055435duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17055435Submitted genomicNC_000012.12:g.262
14137_26214237dup
GRCh38 (hg38)NC_000012.12Chr1226,214,13726,214,237
nssv17055435RemappedPerfectNC_000012.11:g.263
67070_26367170dup
GRCh37.p13First PassNC_000012.11Chr1226,367,07026,367,170

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)
nssv17055435<0.00116404
Support Center