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nsv5464023

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:314,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 855 SVs from 66 studies. See in: genome view    
Submitted genomic110,989,807-111,303,807Question Mark
Overlapping variant regions from other studies: 857 SVs from 66 studies. See in: genome view    
Remapped(Score: Perfect):110,325,506-110,639,505Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5464023Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5110,989,807111,303,807
nsv5464023RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5110,325,506110,639,505

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16973650deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16973650Submitted genomicNC_000005.10:g.110
989807_111303807de
l
GRCh38 (hg38)NC_000005.10Chr5110,989,807111,303,807
nssv16973650RemappedPerfectNC_000005.9:g.1103
25506_110639505del
GRCh37.p13First PassNC_000005.9Chr5110,325,506110,639,505

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)
nssv16973650<0.00116404
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