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nsv5441156

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:84,172

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 350 SVs from 47 studies. See in: genome view    
Submitted genomic218,142,455-218,226,626Question Mark
Overlapping variant regions from other studies: 350 SVs from 47 studies. See in: genome view    
Remapped(Score: Perfect):219,007,178-219,091,349Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5441156Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2218,142,455218,226,626
nsv5441156RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2219,007,178219,091,349

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16923876duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16923876Submitted genomicNC_000002.12:g.218
142455_218226626du
p
GRCh38 (hg38)NC_000002.12Chr2218,142,455218,226,626
nssv16923876RemappedPerfectNC_000002.11:g.219
007178_219091349du
p
GRCh37.p13First PassNC_000002.11Chr2219,007,178219,091,349

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)
nssv16923876<0.00136404
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