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nsv4461638

  • 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: 33 SVs from 10 studies. See in: genome view    
Remapped(Score: Perfect):59,849,322-59,849,322Question Mark
Overlapping variant regions from other studies: 33 SVs from 10 studies. See in: genome view    
Submitted genomic60,314,994-60,314,994Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4461638RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr159,849,32259,849,322
nsv4461638Submitted genomicGRCh37.p13Primary AssemblyNC_000001.10Chr160,314,99460,314,994

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16023622alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16023622RemappedPerfectNC_000001.11:g.598
49322_59849323ins2
81
GRCh38.p12First PassNC_000001.11Chr159,849,32259,849,322
nssv16023622Submitted genomicNC_000001.10:g.603
14994_60314995ins2
81
GRCh37.p13NC_000001.10Chr160,314,99460,314,994

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)
nssv16023622<0.0011021694
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