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nsv5485862

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:352

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 134 SVs from 31 studies. See in: genome view    
Submitted genomic103,088,804-103,089,155Question Mark
Overlapping variant regions from other studies: 134 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):102,729,251-102,729,602Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5485862Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7103,088,804103,089,155
nsv5485862RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7102,729,251102,729,602

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17000553deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17000553Submitted genomicNC_000007.14:g.103
088804_103089155de
l
GRCh38 (hg38)NC_000007.14Chr7103,088,804103,089,155
nssv17000553RemappedPerfectNC_000007.13:g.102
729251_102729602de
l
GRCh37.p13First PassNC_000007.13Chr7102,729,251102,729,602

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)
nssv17000553<0.00136404
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