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nsv4536366

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 36 SVs from 11 studies. See in: genome view    
Remapped(Score: Perfect):209,827,668-209,827,668Question Mark
Overlapping variant regions from other studies: 38 SVs from 11 studies. See in: genome view    
Submitted genomic210,001,013-210,001,013Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4536366RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1209,827,668209,827,668
nsv4536366Submitted genomicGRCh37.p13Primary AssemblyNC_000001.10Chr1210,001,013210,001,013

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16029796insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16029796RemappedPerfectNC_000001.11:g.209
827668_209827669in
s292
GRCh38.p12First PassNC_000001.11Chr1209,827,668209,827,668
nssv16029796Submitted genomicNC_000001.10:g.210
001013_210001014in
s292
GRCh37.p13NC_000001.10Chr1210,001,013210,001,013

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)
nssv160297960.01633921664
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