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nsv5493905

  • 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: 110 SVs from 26 studies. See in: genome view    
Submitted genomic121,366,346-121,366,397Question Mark
Overlapping variant regions from other studies: 110 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):121,006,400-121,006,451Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5493905Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7121,366,346121,366,397
nsv5493905RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7121,006,400121,006,451

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17005003deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17005003Submitted genomicNC_000007.14:g.121
366346_121366397de
l
GRCh38 (hg38)NC_000007.14Chr7121,366,346121,366,397
nssv17005003RemappedPerfectNC_000007.13:g.121
006400_121006451de
l
GRCh37.p13First PassNC_000007.13Chr7121,006,400121,006,451

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)
nssv170050030.002106404
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