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nsv6289756

  • Variant Calls:3
  • 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: 296 SVs from 35 studies. See in: genome view    
Submitted genomic46,110,777-46,110,777Question Mark
Overlapping variant regions from other studies: 296 SVs from 35 studies. See in: genome view    
Remapped(Score: Perfect):47,530,691-47,530,691Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6289756Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2146,110,77746,110,777
nsv6289756RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2147,530,69147,530,691

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17943753insertionSequencingSequence alignment
nssv17948707insertionSequencingSequence alignment
nssv17955116insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17943753Submitted genomicNC_000021.9:g.4611
0777_46110778ins53
GRCh38 (hg38)NC_000021.9Chr2146,110,77746,110,777
nssv17948707Submitted genomicNC_000021.9:g.4611
0777_46110778ins53
GRCh38 (hg38)NC_000021.9Chr2146,110,77746,110,777
nssv17955116Submitted genomicNC_000021.9:g.4611
0777_46110778ins53
GRCh38 (hg38)NC_000021.9Chr2146,110,77746,110,777
nssv17943753RemappedPerfectNC_000021.8:g.4753
0691_47530692ins53
GRCh37.p13First PassNC_000021.8Chr2147,530,69147,530,691
nssv17948707RemappedPerfectNC_000021.8:g.4753
0691_47530692ins53
GRCh37.p13First PassNC_000021.8Chr2147,530,69147,530,691
nssv17955116RemappedPerfectNC_000021.8:g.4753
0691_47530692ins53
GRCh37.p13First PassNC_000021.8Chr2147,530,69147,530,691

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)
nssv179437530.0021598
nssv179487070.49810552118
nssv179551160.0021598
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