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nsv4535623

  • 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: 23 SVs from 6 studies. See in: genome view    
Remapped(Score: Perfect):157,022,512-157,022,512Question Mark
Overlapping variant regions from other studies: 24 SVs from 6 studies. See in: genome view    
Submitted genomic156,992,304-156,992,304Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4535623RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1157,022,512157,022,512
nsv4535623Submitted genomicGRCh37.p13Primary AssemblyNC_000001.10Chr1156,992,304156,992,304

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16027807insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16027807RemappedPerfectNC_000001.11:g.157
022512_157022513in
s281
GRCh38.p12First PassNC_000001.11Chr1157,022,512157,022,512
nssv16027807Submitted genomicNC_000001.10:g.156
992304_156992305in
s281
GRCh37.p13NC_000001.10Chr1156,992,304156,992,304

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)
nssv160278074.6e-005121694
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