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nsv5394191

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 153 SVs from 22 studies. See in: genome view    
Submitted genomic180,983,039-180,983,090Question Mark
Overlapping variant regions from other studies: 155 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):180,952,175-180,952,226Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5394191Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1180,983,039180,983,090
nsv5394191RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1180,952,175180,952,226

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16893009alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16893009Submitted genomicNC_000001.11:g.180
983039_180983090in
s236
GRCh38 (hg38)NC_000001.11Chr1180,983,039180,983,090
nssv16893009RemappedPerfectNC_000001.10:g.180
952175_180952226in
s236
GRCh37.p13First PassNC_000001.10Chr1180,952,175180,952,226

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)
nssv16893009<0.00126404
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