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nsv5507204

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:72

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 88 SVs from 17 studies. See in: genome view    
Submitted genomic103,570,607-103,570,678Question Mark
Overlapping variant regions from other studies: 88 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):105,330,364-105,330,435Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5507204Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10103,570,607103,570,678
nsv5507204RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10105,330,364105,330,435

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17040960deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17040960Submitted genomicNC_000010.11:g.103
570607_103570678de
l
GRCh38 (hg38)NC_000010.11Chr10103,570,607103,570,678
nssv17040960RemappedPerfectNC_000010.10:g.105
330364_105330435de
l
GRCh37.p13First PassNC_000010.10Chr10105,330,364105,330,435

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)
nssv17040960<0.00156404
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